- Research article
- Open Access
Genetic background (DDD/Sgn versus C57BL/6J) strongly influences postnatal growth of male mice carrying the Ayallele at the agouti locus: identification of quantitative trait loci associated with diabetes and body weight loss
BMC Genetics volume 14, Article number: 35 (2013)
Mice carrying the Ay allele at the agouti locus become obese and are heavier than their non-Ay littermates. However, this does not hold true for the genetic background of the DDD mouse strain. At 22 weeks of age, DDD.Cg-Ay females are heavier than DDD females, whereas DDD.Cg-Ay males are lighter than DDD males. This study aimed to determine the possible cause and identify the genes responsible for the lower body weight of DDD.Cg-Ay males.
Growth curves of DDD.Cg-Ay mice were analyzed and compared with those of B6.Cg-Ay mice from 5 to 25 weeks. In DDD.Cg-Ay males, body weight gain stopped between 16 and 17 weeks and the body weight gradually decreased; thus, the lower body weight was a consequence of body weight loss. Quantitative trait locus (QTL) mapping was performed in backcrossed (BC) males of DDD × (B6 × DDD.Cg-Ay) F1-Ay mice. For the body weight at 25 weeks, significant QTLs were identified on chromosomes 1 and 4. The DDD allele was associated with a lower body weight at both loci. In particular, the QTL on chromosome 4 interacted with the Ay allele. Furthermore, suggestive QTLs for plasma glucose and high molecular weight adiponectin levels were coincidentally mapped to chromosome 4. The DDD allele was associated with increased glucose and decreased adiponectin levels. When the body weight at 25 weeks and plasma glucose levels were considered as dependent and independent variables, respectively, BC Ay males were classified into two groups according to statistical analysis using the partition method. Mice of one group had significantly higher glucose and lower adiponectin levels than those of the other group and exhibited body weight loss as observed with DDD-Ay males.
The lower body weight of DDD.Cg-Ay male mice was a consequence of body weight loss. Diabetes mellitus has been suggested to be a possible contributory factor causing body weight loss. The QTL on distal chromosome 4 contained the major responsible genes. This QTL interacted with the Ay allele, implying the reason why body weight loss occurs in DDD.Cg-Ay but not in DDD males.
Traditionally, five single gene obesity mutations, Cpefat, Tubtub, Lepob, Leprdb, and Ay, have been identified in mice . Among these, only the Ay allele is dominant and homozygous lethal; therefore, living Ay mice are invariably heterozygotes. Obesity in Ay mice is moderate and occurs late compared with that in the other four mutants. Ay mice also show metabolic abnormalities such as hyperglycemia and marked hyperinsulinemia, making them a suitable animal model system for studying obesity-associated diabetes mellitus in humans.
In normal mice, the agouti gene is expressed only in the skin [2, 3], and it regulates pigmentation by acting as an inverse agonist of the melanocortin 1 receptor [4, 5]. However, in Ay mice, the Ay allele is associated with a large deletion, which causes agouti gene expression to be aberrantly controlled by the unrelated Raly gene promoter and results in its ectopic overexpression [3, 6–8]. Thus, Ay mice have a yellow coat color and develop maturity-onset obesity. Obesity in Ay mice is thought to be a consequence of the agouti protein acting as a constitutive antagonist of the melanocortin 3 receptors (MC3R) and melanocortin 4 receptor (MC4R) by mimicking the actions of the agouti-related protein [9–11].
Till date, two mouse strains congenic for the Ay allele are available: B6.Cg-Ay (C57BL/6J background; hereafter B6-Ay) and KK.Cg-Ay (KK/Ta background; hereafter KK-Ay). We developed a third mouse strain congenic for the Ay allele in an inbred DDD/Sgn (hereafter DDD) strain background, (i.e., DDD.Cg-Ay; hereafter DDD-Ay) . DDD-Ay females are significantly obese compared with B6-Ay and KK-Ay females .
From our previous observations, DDD-Ay females (average body weight of 62.1 g at 22 weeks) are heavier than DDD females (37.6 g), whereas DDD-Ay males (36.0 g) are lighter than DDD males (40.4 g). Surprisingly, within a DDD background, the Ay allele increased the female body weight, whereas it reduced the male body weight. Within B6 and KK backgrounds, Ay males are heavier than their non-Ay male littermates.
To confirm this unusual phenomenon, we conducted additional detailed analyses of the body weight and growth in the DDD-Ay strain in comparison with those in B6-Ay and reciprocal F1 strains. We also conducted some pathophysiological analyses to determine possible causes of the lower body weight. In addition, we conducted quantitative trait locus (QTL) mapping analysis to identify genes associated with the lower body weight within the DDD background based on the assumption that the lower body weight was a heritable phenomenon.
The inbred DDD mouse strain was maintained at the National Institute of Agrobiological Sciences (NIAS, Tsukuba, Ibaraki, Japan). The inbred B6 mouse strain was purchased from Clea Japan, Inc. (Tokyo, Japan), and the congenic B6-Ay mouse strain was purchased from the Jackson Laboratory (Bar Harbor, ME, USA). The congenic DDD-Ay mouse strain was established by introgression of the Ay allele from the B6-Ay strain into the DDD strain by backcrossing for 12 generations. Because the original DDD strain had an albino coat, congenic DDD-Ay mice were further intercrossed between yellow (Ay) and agouti (A) littermates to eliminate the Tyrc allele.
In this study, agouti littermates were used as DDD control mice. Hereafter, DDD-Ay and B6-Ay are collectively referred to as Ay mice. Likewise, their control littermates, DDD and B6, were designated as non-Ay mice. Mice homozygous for the Ay allele were embryonic lethal; thus, all Ay mice used in this study were heterozygotes. Ay mice were distinguishable from non-Ay mice because Ay mice had yellow coats (as opposed to non-Ay mice with agouti or black coats).
We also analyzed reciprocal F1 mice produced by a cross between DDD (−Ay) and B6 (−Ay) strains. (♀DDD × ♂B6-Ay) F1 mice were designated DB, and (♀B6 × ♂DDD-Ay) F1 were designated BD. Following the designations of inbred strains, DB-Ay and BD-Ay mice were referred to as Ay mice and their agouti littermates were referred to as non-Ay mice. The mouse strain designations used in this study are summarized in Table 1.
Mice were weaned at 4 weeks of age, and 4–5 mice were housed together during the experimental period. All the mice were maintained in a specific pathogen-free facility with a regular light cycle and controlled temperature and humidity. Food (CRF-1; Oriental yeast Co. Ltd., Tokyo, Japan) and water were freely available throughout the experimental period. All the animal experiments were conducted in accordance with the guidelines of the Institutional Animal Care and Use Committee of NIAS.
Body weight measurements and growth analysis
Body weights were weekly measured from 5 to 25 weeks of age and were determined to the nearest 0.01 g using an electronic balance. The average body weights of mice from 5 to 25 weeks were modeled as the study outcomes using the following three equations:
Eqs. 1 and 2 are known as the von Bertalanffy growth model  and the elasticity model , respectively. In Eq. 1, the body weight at birth was assumed to be zero and the growth rate was considered to be proportional to the maximum size minus the current size. Thus, the body weight reached an upper limit value over time. In Eq. 2, elasticity was a coefficient estimated from a linear regression equation where both dependent and independent variables were presented as natural logs. In this model, the growth rate was proportional to the current ratio of the body weight to age. In Eq. 3, we added a quadratic term to Eq. 2 to fit the curves better to the observed data. In Eqs. 2 and 3, the body weight was expressed as Exp (a) at 1 week of age using the value of parameter a.
For these analyses, the independent variable of time was treated as a continuous variable and mouse characteristics (strain, agouti, sex, and their interactions) were treated as nominal variables.
For the agouti genotype (i.e., whether the mouse had the Ay allele), mice with or without the Ay allele were designated Y and A, respectively. With regard to sex, males and females were designated M and F, respectively. With regard to strains, mice were classified into one of the following four strains: DDD, B6, BD, and DB. Agouti, sex, and strain were used as independent variables and designated Strain*Agouti*Sex. All the mice were classified into one of the following 16 categories: DDDYM, DDDYF, DDDAM, DDDAF, B6YM, B6YF, B6AM, B6AF, DBYM, DBYF, DBAM, DBAF, BDYM, BDYF, BDAM, and BDAF.
In this study, growth models were designated models 1, 2, and 3, as described by Eqs. 1, 2, and 3, respectively. Each of the 16 Strain*Agouti*Sex categories was analyzed using the three models. In model 1, the maximum likelihood estimates for parameter values were obtained by minimizing the deviance in the observed data by weighting by the number of mice. The 95% confidence intervals (CIs) were determined using the profile likelihood. In models 2 and 3, the optimum estimates and 95% CI for the parameters were determined using the least-squares method weighted by the number of mice. Statistical significance was set at the α = 0.05 level. Data analysis used JMP ver. 9.0.1 statistical software (SAS Institute Inc., Cary, NC, USA).
Blood phenotype analyses
At 25 weeks of age, mice were euthanized with an overdose of ether after they were fasted for 4 h. Whole blood was drawn from the heart into a plastic tube using heparin as an anticoagulant. Blood glucose (BGLC) levels were then determined using Glutest Pro R (Sanwa Kagaku Kenkyusho, Aichi, Japan) according to the manufacturer’s instructions. Sample tubes were centrifuged at 7,000 rpm for 5 min at 4°C to separate plasma. The plasma samples were maintained at −70°C until use. Plasma glucose (PGLC) levels were determined using a clinical colorimetric kit (Glucose C-II Test Wako, Wako Pure Chemical Industries, Osaka, Japan). Plasma total-cholesterol (CHO) and triglyceride (TG) levels were determined using Cholesterol E Test Wako and Triglyceride E Test Wako (Wako Pure Chemical Industries). Plasma high-molecular-weight adiponectin (HMW adiponectin) levels were determined using the Mouse/Rat High Molecular Weight Adiponectin ELISA Kit (AKMAN-011, Shibayagi, Gunma, Japan). For statistical comparisons between groups, the Tukey–Kramer honestly significant difference (HSD) test was used. P values <0.05 were considered statistically significant.
The liver, pancreas, and adipose tissues were removed at necropsy from parental strains of both the sexes. Formalin-fixed tissues were embedded in paraffin, sectioned, and stained with hematoxylin and eosin.
The anal–nasal length of each mouse was measured using a pair of digital calipers to the nearest 0.01 mm just after blood collection to avoid rigor mortis. Body length was defined as the anal–nasal length. Body mass index (BMI) was calculated as follows: body weight (g)/[body length (mm)]2 × 103. BMI was used to estimate the degree of obesity.
QTL mapping analysis was conducted to identify genes possibly associated with the lower body weight of DDD-Ay males. We produced 196 backcross (BC) males, comprising 100 Ay (BC Ay) and 96 non-Ay (BC non-Ay) males, from a genetic cross of ♀DDD × ♂(♀B6 × ♂DDD-Ay) F1-Ay mice. This backcrossing was chosen because neither BD-Ay males nor DB-Ay males showed body weight loss and the DDD alleles involved in this phenomenon were considered to be recessive to the B6 allele. QTL analysis was primarily conducted in 100 BC Ay males; 96 BC non-Ay males were genotyped for all markers on chromosomes 1 and 4.
Genomic DNA isolation and genotyping of microsatellite markers used the procedures described in our previous study . Microsatellite markers used in this study are listed in Table 2 with their map positions (cM) calculated using 196 BC males. X chromosome-linked markers were not genotyped because they were not informative with this genetic cross.
Notably, chromosome 7 is divided into two parts. Because of the introgression of the Tyr locus from the B6 strain, an intermediate part of the DDD genome on chromosome 7 is replaced by a B6 genome in DDD-Ay mice. In this study, a region proximal to the B6 region was defined as “chromosome 7.1 (D7Mit250)” whereas a region distal to the B6 region was defined as “chromosome 7.2 (D7Mit362).”
QTL analysis was conducted using R/qtl [16, 17]. Threshold logarithm of odds (LOD) scores for suggestive (P < 0.63) and significant (P < 0.05) linkages were determined by performing 1,000 permutations for each trait . For significant QTLs, 95% CI was defined by a decline of 1.5 LOD. After single QTL scans, pairwise evaluations for potential interactions between loci were made. At this stage, threshold LOD scores were strictly based on those recommended by Broman and Sen .
To determine whether the effect of QTL was specifically identified in the presence of the Ay allele, data for BC Ay and BC non-Ay mice were combined and reanalyzed using the agouti locus genotype as a covariate. Because the difference between the LOD score with the agouti locus genotype as an interactive covariate and the LOD score with the agouti locus genotype as an additive covariate concerns the test of the QTL × agouti locus genotype interaction, this test was performed for combined BC mice.
After QTL mapping, we genotyped interferon activated gene 202B (Ifi202b) and zinc finger protein 69 (Zfp69) to test their suitability as candidate genes for the QTLs.
Statistical analysis using a linear model and partition method
Body weights of BC Ay males at 25 weeks of age were used as the dependent variable in the linear model and partition method with JMP ver. 9.0.1 statistical software. PGLC, CHO, TG, and HMW adiponectin levels were independent variables and treated as continuous variables. The best-fit linear model was generated from a full model by reducing nonsignificant terms using stepwise procedures. In the partition method, PGLC levels were used as an independent variable. We stopped first or second splits because of the small sample size. The clusters split in the partition method were treated as independent nominal variables. Comparisons of the associations between the clusters and other dependent variables (e.g., body weight at 25 weeks, BMI, PGLC, CHO, TG, and HMW adiponectin levels) were made by an F-test, followed by Student’s or Welch’s test. P values <0.05 was considered statistically significant. The average body weights of BC Ay males clustered in the partition method were modeled from 5 to 25 weeks of age using model 3 described by Eq. 3.
Growth of DDDYM mice stops between 16 and 17 weeks, following which body weight gradually declines
Figure 1 shows the growth curves of the parental inbred mouse strains (A, males; B, females) and F1 mice (C, males; D, females) from 5 to 25 weeks of age. The corresponding growth curve analytic results are shown in Table 3. Growth curve data were best fit to model 3 for 10 of 16 mouse categories: B6AF, B6AM, B6YF, B6YM, BDYF, BDYM, DBYM, DDDAF, DDDYF, and DDDYM. Growth curve data were best fit to model 2 for the remaining six categories: BDAF, BDAM, DBAF, DBAM, DBYF, and DDDAM. The fits of the observed data to all the three models were statistically significant (P < 0.05).
In model 1, the maximum body weight ranged from 24.8 g (B6AF mice) to 72.3 g (DDDYF mice). In non-Ay mice, the maximum body weight of males was greater than that of females within the same strain. In contrast, in Ay mice, the maximum body weight of females was greater than that of males within the same strain. The growth rate was the greatest in DDDYM mice (0.292). The body weight of DDDYM mice reached the maximum value at the earliest age. The difference in the maximum body weight between males and females was the greatest in DDDY mice (28.9 g) (Figure 2A).
In accordance with the results with model 1, the growth rate was the lowest in DDDYM mice (0.133) in model 2. The adjusted R-squared value was the smallest in DDDYM mice (0.670). The adjusted R-squared values for the other categories were >0.900.
In model 3, DDDYM mice reached their maximum body weights (mean = 43.5 g) at 16.7 weeks of age (Figure 2B). The maximum body weight of DDDYM mice was nearly equal to that obtained in model 1 (mean = 43.4 g). The body weights of the other mouse categories did not reach the maximum values during the observation period. The values for the parameter c were positive in BDAF, DBAF, and DBAM mice, but were negative in the remaining 13 categories. The smallest value for the parameter c was found in DDDYM mice (−0.195).
Blood phenotypes of DDD-Aymales
We determined the BGLC, CHO, TG, and HMW adiponectin levels in parental strains at 25 weeks of age. The first three levels were also determined for F1 mice. DDD-Ay and DB F1-Ay males had significantly higher BGLC levels than mice with other genotypes. No significant differences in BGLC levels were observed between DDD-Ay and DB F1-Ay males (Figure 3A). DDD-Ay and DDD mice clearly had higher TG levels than B6-Ay and B6 mice for both the sexes (Figure 3B). In particular, DDD-Ay males had significantly higher TG levels than the other strains, except for DB F1-Ay males. In contrast, DDD-Ay and DDD mice were not hypercholesterolemic compared with B6-Ay and B6 mice, respectively, for both the sexes (Figure 3C). Conversely, DDD-Ay males had significantly lower CHO levels than DDD and B6-Ay males. DDD-Ay males had significantly lower HMW adiponectin levels than B6-Ay, B6, and DDD males (Figure 3D).
No marked abnormalities were observed in the pancreas and adipose tissues of any of the mice. Liver lesions were observed only in Ay mice, although these were found in both the sexes. Indeed, fatty changes were observed in DDD-Ay and B6-Ay males, while glycogen deposition was observed in DDD-Ay and B6-Ay females. Deposition of large fat droplets was observed in DDD-Ay and B6-Ay females (data not shown).
QTLs associated with lower body weight of DDD.Cg-Aymales are identified on chromosomes 1 and 4
We conducted QTL analyses for body weight (from 5 to 25 weeks of age), BMI, and BGLC, PGLC, CHO, TG, and HMW adiponectin levels using the results of 100 BC Ay males. Seven BC Ay males had BGLC levels of >600 mg/dl, the upper limit of detection for the method used. Their BGLC levels were assumed to be 600 mg/dl. To make glucose determination more exact, we also measured PGLC levels; PGLC levels were highly correlated with BGLC levels (r = 0.95; P <0.0001). Phenotypes are shown in Table 4 along with those for 96 BC non-Ay males. Phenotypic values were significantly greater in BC Ay males than in BC non-Ay males (PGLC and HMW adiponectin levels were not determined in BC non-Ay males).
The results of single QTL scans are summarized in Table 5. For the body weight at 25 weeks of age, two significant QTLs were identified on chromosomes 1 and 4 (Figure 4). For 21 QTL analyses of body weight conducted weekly (from 5 to 25 weeks), significant QTLs were identified only on chromosomes 1 and 4. QTL results for chromosome 1 were significant only for body weight at 25 weeks of age (Figure 5). In contrast, QTL results for chromosome 4 were significant from 14 weeks onward, except at 16 weeks. For both QTLs, the DDD allele was associated with a lower body weight (Figure 6).
For BMI, one significant QTL was identified on chromosome 4 (Figure 4). For this QTL, the DDD allele was associated with lower BMI. Suggestive QTLs for HMW adiponectin, BGLC, and PGLC levels were colocalized with the QTL for body weight on chromosome 4 but not with the QTL on chromosome 1 (Figure 7). The DDD allele was associated with increased BGLC and PGLC levels and decreased HMW adiponectin levels (Figure 8). For BGLC and PGLC, suggestive QTLs were also identified on chromosomes 7.1 and 12. At both loci, the B6 allele was associated with increased glucose levels. Three suggestive QTLs were identified for TG levels on chromosomes 8, 12, and 18 (Figure 9). The suggestive QTL on chromosome 12 coincided with the suggestive QTLs for BGLC and PGLC levels. The DDD allele was associated with increased TG levels. No significant or suggestive QTLs were identified for CHO levels. The effects of the loci on chromosomes 1 and 4 for TG and CHO levels were negligible.
We next addressed whether the effects of QTLs on chromosomes 1 and 4 could be identified in the absence of the Ay allele (i.e., in BC non-Ay males), i.e., whether or not QTLs on chromosomes 1 and 4 interacted with the Ay allele. When QTL analysis of body weight at 25 weeks of age was conducted for 96 BC non-Ay males, there was no evidence of linkage with regard to chromosomes 1 and 4 (Figure 10). When BC Ay and BC non-Ay males were combined and reanalyzed using the agouti locus genotype (Ay or non-Ay) as a covariate, significant evidence of a QTL × covariate interaction was identified for the QTL on chromosome 4 but not for the QTL on chromosome 1 (Table 6 and Figure 11). Thus, the effect of the QTL on chromosome 4 differed between in BC Ay and in BC non-Ay males, i.e., the effect of this QTL differed between in the presence and absence of the Ay allele (Figure 6B).
We further mapped these QTLs using a reference map position retrieved from Mouse Genome Informatics (MGI, http://www.informatics.jax.org/) in order to search possible candidate genes for the QTLs. For this purpose, we excluded genotype data on D1Mit16 and D4Mit234 because information on Mbp position was not available for these markers. Instead, we newly genotyped D1Mit36 (169.21 Mbp), D1Mit356 (172.89 Mbp), D1Mit155 (194.43 Mbp), and D4Mit204 (133.43 Mbp). Results of single QTL scans for body weight at 25 weeks are summarized in Table 7. The 95% CI for QTLs on chromosomes 1 and 4 contained plausible candidate genes, Ifi202b and Zfp69, respectively, both of which were known to be related with obesity-associated diabetes [19, 20].
Therefore, we genotyped Ifi202b and Zfp69 to test their suitability as candidate genes for the QTLs. For the genotyping of Ifi202b, we performed two kinds of PCR using cDNA as a template . As shown in Figure 12A and Table 8, forward primer corresponding to the corresponding to the exon 1B (F1), which was missing in B6, in combination with reverse primers on exon 3 (R1) and 2 (R2) amplified a PCR product only on DDD cDNA (Figure 12B and Figure 12C, respectively). For the genotyping of Zfp69, we performed PCR using cDNA as a template . As shown in Figure 13A and Table 8, forward primer corresponding to the exon 3 (F2) in combination with reverse primer on B6-specific exon 3A (R3) amplified a PCR products on B6 and DDD (Figure 13B). We also performed PCR using unrelated RR/Sgn strain but it did not generate a PCR product.
Statistical analysis with a linear model and partition method
The best-fit linear model was as follows:
In Eq. 4, PGLC and HMW adiponectin levels were linearly related to the body weight and the square of PGLC levels was related to the body weight. Estimates for the four parameters were as follows: a = 32.4, b =0.068, c = 1.06, and d = −7.5×10−5. The adjusted R-squared value and the root mean square error were 0.255 and 4.37 g, respectively. Body weight at 25 weeks of age increased in direct proportion to HMW adiponectin levels. Figure 14A shows the association between the observed body weights at 25 weeks of age and the predicted body weights from Eq. 4. The predicted body weight reached a maximum (51.9 g) at the point when the PGLC level was 427.3 mg/dl.
When the body weight at 25 weeks of age was used as the dependent variable, BC Ay males were categorized into two groups with the first split of the partition method. The first group included nine mice with PGLC levels ≥715 mg/dl, and the second group included 91 mice with PGLC levels <715 mg/dl. The average body weight of the first group was 41.2 g and that of the second group was 50.2 g. We defined the first group as “abnormal mice” and the second group as “normal mice.” Abnormal mice were characterized by higher PGLC levels and lower HMW adiponectin levels compared with normal mice.
In Figure 14A, the nine abnormal mice were mapped to the lower right of the plot area, in which mice had PGLC levels ≥715 mg/dl and body weights ranging from 37.4 g to 43.8 g. Comparisons of the phenotypes between these two groups are summarized in Table 9. Body weight, BMI, BGLC levels, PGLC levels, and HMW adiponectin levels significantly differed between these abnormal and normal mice. In contrast, CHO and TG levels did not differ significantly between these two groups.
Figure 14B shows a comparison of the growth curves of abnormal and normal mice using model 3. For abnormal mice, estimates for the three parameters in this model were a = 1.33, b = 1.82, and c = −0.34. For normal mice, these estimates were a = 1.45, b = 1.56, and c = −0.25. The adjusted R-squared value and the root mean square errors were 0.99 and 0.016, respectively. The average body weight of abnormal mice was greater than that of normal mice until 10.7 weeks. Following this, body weight trends reversed between these two groups; normal mice became heavier than abnormal mice. Abnormal mice reached their maximum body weight (45.2 g) at 15.1 weeks of age, following which their body weight declined.
Growth of DDDYM mice was peculiar among the 16 categories, and the lower body weight of the DDDYM mice was a consequence of body weight loss
From the results of model 1, the maximum body weight of males was greater than that of females of the same strain in non-Ay mice (Table 3). The maximum body weight of 46.9 g in DDDAM mice was greater than that of 39.7 g in DDDAF mice. In contrast, the maximum body weight of females was greater than that of males of the same strain in Ay mice. The maximum body weight of 72.3 g in DDDYF mice was greater than that of 43.4 g in DDDYM mice. The greatest maximum body weight of non-Ay mice was lesser than the smallest maximum body weight of Ay mice, which indicated that the Ay allele had a strong effect on growth irrespective of strain or sex.
Because the maximum body weight of 50.9 g in B6YM mice was greater than that of 33.3 g in B6AM mice, the maximum body weight of DDDYM mice should have been greater than that of DDDAM mice. However, the maximum body weight of DDDYM mice was lesser than that of DDDAM mice. In model 3, the growth of DDDYM mice stopped between 16 and 17 weeks, following which their body weight declined. In contrast, the body weight of DDDYF mice continued to increase during the observation period (Figure 2B).
Based on these results, we concluded that the growth of DDDYM mice was quite peculiar among the 16 categories of mice used in this study. This peculiar growth was supported by the following evidence: (1) among the 16 categories of mice, the growth rate was the greatest using model 1; (2) the adjusted R-squared value was the smallest using model 2; and (3) the quadratic term [Log(Week)]2 was the smallest using model 3. Most importantly, DDDYM mice attained their maximum body weight at 16.7 weeks of age, following which their body weight declined. Mice in the other 15 categories did not attain their maximum body weights during the observation period. Therefore, the lower body weight of DDDYM mice was a consequence of body weight loss.
Diabetes mellitus is a possible cause of body weight loss in DDD-Aymales
Diabetes and obesity are common characteristics of Ay mice. Hyperglycemia/type 2 diabetes is a possible reason for body weight loss in these mice. Therefore, BGLC levels were determined to address this possibility. DDD-Ay males showed marked hyperglycemia (Figure 3A). DB F1-Ay males also showed hyperglycemia but did not lose their body weight, suggesting that hyperglycemia was not the sole cause of body weight loss. Because body weight loss and hyperglycemia were not observed in BD F1-Ay males, loci homozygous for DDD alleles must have caused the body weight loss and the maternally derived DDD genome must have induced hyperglycemia.
We also determined plasma lipid levels because dyslipidemia is frequently associated with diabetes and obesity. Clearly, DDD-Ay and DDD mice had higher plasma TG levels than B6-Ay and B6 mice for both the sexes (Figure 3B). In particular, DDD-Ay males had significantly higher plasma TG levels than the other strains, except for DB F1-Ay males. In contrast, DDD-Ay and DDD mice were not more cholesterolemic compared with B6-Ay and B6 mice for both the sexes (Figure 3C). Conversely, DDD-Ay males had significantly lower plasma CHO levels than DDD and B6-Ay males.
We determined HMW adiponectin levels in parental strains. Adiponectin is an adipokine secreted from adipose tissues and is known to reverse insulin resistance associated with obesity by stimulating glucose utilization and fatty-acid oxidation [21, 22]. Disrupting adiponectin production and/or release causes insulin resistance and increases serum TG levels but not serum CHO levels . Blood HMW adiponectin levels more definitively reflect BMI, the effect of body weight loss, glucose tolerance, insulin sensitivity in the liver, metabolic syndrome, and type 2 diabetes mellitus than the levels of total adiponectin. Clearly, HMW adiponectin levels were significantly reduced in DDD-Ay males.
We also performed histological examinations for possible abnormalities associated with body weight loss. Liver lesions are possible associated with the advancement of obesity. Unexpectedly, liver lesions were more severe in B6-Ay mice than in DDD-Ay mice. In addition, in our earlier observation, we detected enlarged kidneys as a consequence of dilatation of the renal pelvis in DDD-Ay males; however, we failed to confirm this in a subsequent study. Dilatation of the renal pelvis immediately suggested that the enlarged kidney could be caused by hydronephrosis. Nakajima et al.  reported a high incidence of hydronephrosis in DDD males, although they did not report any evidence of body weight loss. According to Goto et al. , hydronephrosis in DDD mice is heritable and probably controlled by polygenes. Although our DDD strain was a descendant of the DDD strain used by Nakajima et al.  and Goto et al. , we did not observe hydronephrosis in our DDD strain. Overall, we could not find any histological evidence that may be associated with body weight loss in DDD-Ay males.
Based on these observations, we concluded that DDD-Ay males suffered from diabetes mellitus.
Body weight loss is heritable and controlled by a major QTL on chromosome 4
When the agouti locus genotype was included as a covariate, a significant QTL × covariate interaction was identified on chromosome 4. The importance of this QTL was that it was significant for body weight and BMI and it interacted with the Ay allele. That is, the action of this QTL differed between BC non-Ay and BC Ay males, which suggested a reason why body weight loss occurred in DDD.Cg-Ay males but not in DDD males. This QTL was also important because it was suggestive QTLs for HMW adiponectin levels and BGLC and PGLC levels. The DDD allele was associated with decreased body weight, BMI, and HMW adiponectin levels and increased BGLC and PGLC levels, suggesting that the QTL on chromosome 4 was responsible for diabetes mellitus. For PGLC, a larger QTL effect was identified on chromosome 12. However, this QTL was unlikely to be a direct cause of hyperglycemia of DDD.Cg-Ay males because the B6 allele was associated with increased glucose level at this locus. It was uncertain whether this locus was allelic with that for TG levels because the B6 allele was associated with decreased TG levels.
The QTL on chromosome 1 contained Ifi202b and the QTL on chromosome 4 contained Zfp69 within the 95% CI as a strong candidate gene [19, 20]. Ifi202b was identified as a cause of Nob3, a major QTL for obesity and hyperglycemia in an F2 intercross between NZO and B6 mouse strains . In B6 mice, Ifi202b is disrupted by a deletion of its 5’-flanking region including exon 1B and the promoter . According to the PCR analysis, the DDD strain had exon 1B as opposed to B6 allele. There is no reason to exclude Ifi202b as a candidate gene for the QTL on chromosome 1; however, we are still uncertain whether the QTL on chromosome 1 is allelic to Nob3 because of following reasons. First, the phenotypic effect of the QTL on chromosome 1 on body weight, BGLC, and PGLC was apparently weak as compared with Nob3. Second, the B6 allele was associated with increased body weight at the present QTL, whereas the B6 allele was associated with decreased body weight in (NZO × B6) F2 population.
On the other hand, Zfp69 was identified as a cause of Nidd/SJL in a backcross male progeny between NZO and SJL strains . The Zfp69 gene is disrupted in B6 and NZO strains by an insertion of a retrotransposon sequence [20, 28]. Intriguingly, disrupted allele protects mice against diabetes. Thus, in a cross between NZO and SJL mice, the wild-type SJL allele contributed to diabetes. The SJL allele at Nidd/SJL was associated with decreased body weight and BMI and increased BGLC and TG levels. In the similar way as did the SJL allele at Nidd/SJL, the DDD allele at the QTL on chromosome 4 was associated with decreased body weight and BMI and increased BGLC, suggesting the allelism between the two QTLs, However, our results of Zfp69 genotyping suggested that the exon 3A was present in the DDD strain, and that there were no differences between the B6 and DDD alleles. In addition, we sequenced all exons except for exon 3A in the DDD strain and found there were no differences between the B6 and DDD alleles (data not shown). Different from the effects associated with Nidd/SJL, the QTL on chromosome 4 in our cross did not have any substantial effects on TG levels. Thus, the QTL on chromosome 4 was unlikely to be caused by the Zfp69. However, this by no means rule out the possibility that the Zfp69 plays a role in parental DDD.Cg-Ay males because the diabetogenic effect of the Zfp69 variant is markedly dependent on interaction with other genes of the background strain .
With regard to the QTL on chromosome 4, we can postulate two other candidate genes that are closely related to body weight and diabetes mellitus. One is coristatin (Cort), which is located at 149.13 Mbp . Although the body weight and blood glucose levels did not significantly differ between Cort deficient (Cort−/−) and wild type (Cort+/+) mice, Cort−/− males, but not females, showed insulin resistance during insulin tolerance test. The other candidate gene is hexose-6-phosphate dehydrogenase (H6pd), which is located at 150 Mbp . Fasting glucose level was significantly lower in H6pd deficient (H6pd−/−) mice compared with wild type (H6pd+/+) mice. At 10 weeks of age, H6pd−/− mice were significantly lighter than H6pd+/+ mice. These are undoubtedly candidate genes for the QTL; however, we are still uncertain whether they are causative of the QTL because the effect of the QTL on chromosome 4 is only apparent in the presence of the Ay allele. That is, we cannot correctly assess their candidacy unless these mutant phenotypes are investigated in the presence of the Ay allele.
PGLC and HMW adiponectin levels are critical factors that affect the body weight of BC Aymales
Our best-fit linear model included PGLC and HMW adiponectin levels as linear or quadratic terms, which suggested that PGLC and HMW adiponectin levels were critical factors that affected body weights of BC Ay males as opposed to CHO and TG levels. These results were in accordance with those of our QTL analyses.
Based on partition method analysis, nine abnormal BC Ay males exhibited body weight loss similar to DDD-Ay males. Furthermore, the trajectory of the growth curve of abnormal BC Ay males was very similar to that of DDD-Ay males. This suggested that body weight loss in abnormal BC Ay males was caused by the same factors that contributed to body weight loss in DDD-Ay males. When the phenotypes were compared between the two groups of BC Ay males, body weight, BMI, BGLC, PGLC, and HMW adiponectin levels significantly differed between abnormal and normal mice. In contrast, CHO and TG levels did not differ significantly between these two groups. This suggests again that PGLC and HMW adiponectin levels are critical factors that affect the body weight of BC Ay males. Furthermore, the nine abnormal BC Ay males and DDD-Ay males may have shared the same genetic basis for body weight loss because seven of the nine abnormal BC Ay males were homozygous for the DDD allele at D4Mit234, a microsatellite marker closest to the QTL on chromosome 4.
QTL on chromosome 4 as a modifier of the Ayallele
As mentioned at the beginning of the Background section, five single gene obesity mutations are known at present. These mutations cause obesity and diabetes in mice. The phenotypic effects of these mutations are very strong; nevertheless, the phenotypes caused by these mutations are substantially influenced by the genetic backgrounds on which these mutations are placed [31–36]. In particular, Coleman et al. [31–33] studied the effects of the Lepob and Leprdb mutations on B6 and C57BL/KsJ (KSJ) backgrounds and developed the concept of the diabetes-sensitive and the diabetes-resistant backgrounds. B6 is the resistant background to diabetes associated with obesity caused by the Lepob and Leprdb mutations, whereas KSJ is the diabetes-sensitive background. Similarly, if we assume that DDD is the sensitive background, B6 is again defined as the resistant background to diabetes associated with obesity caused by the Ay allele. Therefore, the QTLs on chromosomes 1 and 4 are expected to encode genes that constitute the diabetes-sensitive genetic background.
Lower body weight of DDD.Cg-Ay males was confirmed to be a consequence of body weight loss. Although we did not yet establish convincing evidence, diabetes mellitus was suggested to be a possible contributing factor that caused body weight loss. Body weight loss was a heritable phenomenon, and a QTL on distal chromosome 4 was suggested to be a major factor responsible for this. This QTL interacts with the Ay allele, suggesting a reason why body weight loss occurs in DDD.Cg-Ay males but not in DDD males.
Leibel RL, Chung WK, Chua SC: The molecular genetics of rodent single gene obesities. J Biol Chem. 1997, 272: 31937-31940. 10.1074/jbc.272.51.31937.
Bultman SJ, Michaud EJ, Woychik RP: Molecular characterization of the mouse agouti locus. Cell. 1992, 71: 1195-1204. 10.1016/S0092-8674(05)80067-4.
Miller MW, Duhl DM, Vrieling H, Cordes SP, Ollmann MM, Winkes BM, Barsh GS: Cloning of the mouse agouti gene predicts a secreted protein ubiquitously expressed in mice carrying the lethal yellow mutation. Genes Dev. 1993, 7: 454-467. 10.1101/gad.7.3.454.
Robbins LS, Nadeau JH, Johnson KR, Kelly MA, Roselli-Rehfuss L, Baack E, Mountjoy KG, Cone RD: Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function. Cell. 1993, 72: 827-834. 10.1016/0092-8674(93)90572-8.
Lu D, Willard D, Patel IR, Kadwell S, Overton L, Kost T, Luther M, Chen W, Woychik RO, Wilkison WO, Cone RD: Agouti protein is an antagonist of the melanocyte-stimulating-hormone receptor. Nature. 1994, 371: 799-802. 10.1038/371799a0.
Duhl DM, Vrieling H, Miller KA, Wolff GL, Barsh GS: Neomorphic agouti mutations in obese yellow mice. Nat Genet. 1994, 8: 59-65. 10.1038/ng0994-59.
Michaud EJ, Bultman SJ, Stubbs LJ, Woychik RP: The embryonic lethality of homozygous lethal yellow mice (Ay/Ay) is associated with the disruption of a novel RNA-binding protein. Genes Dev. 1993, 7: 1203-1213. 10.1101/gad.7.7a.1203.
Michaud EJ, Bultman SJ, Klebig ML, van Vugt MJ, Stubbs LJ, Russell LB, Woychik RP: A molecular model for the genetic and phenotypic characteristics of the mouse lethal yellow (Ay) mutation. Proc Natl Acad Sci USA. 1994, 91: 2562-2566. 10.1073/pnas.91.7.2562.
Chen AS, Marsh DJ, Trumbauer ME, Frazier EG, Guan XM, Yu H, Rosenblum CI, Vongs A, Feng Y, Cao L, Metzger JM, Strack AM, Camacho RE, Mellin TN, Nunes CN, Min W, Fisher J, Gopal-Truter S, MacIntyre DE, Chen HY, Van der Ploeg LH: Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass. Nat Genet. 2000, 26: 97-102. 10.1038/79254.
Huszar D, Lynch CA, Fairchild-Huntress V, Dunmore JH, Fang Q, Berkemeier LR, Gu W, Kesterson RA, Boston BA, Cone RD, Smith FJ, Campfield LA, Burn P, Lee F: Targeted disruption of the melanocortin-4 receptor results in obesity in mice. Cell. 1997, 88: 131-141. 10.1016/S0092-8674(00)81865-6.
Ollmann MM, Wilson BD, Yang YK, Kerns JA, Chen Y, Gantz I, Barsh GS: Antagonism of central melanocortin receptors in vitro and in vivo by agouti-related protein. Science. 1997, 278: 135-138. 10.1126/science.278.5335.135.
Suto J: The Ay allele at the agouti locus reduces the size and alters the shape of the mandible in mice. Proc Jpn Acad Ser B. 2009, 85: 248-257. 10.2183/pjab.85.248.
Suto J: Quantitative trait loci that control body weight and obesity in an F2 intercross between C57BL/6J and DDD.Cg-Ay mice. J Vet Med Sci. 2011, 73: 907-915. 10.1292/jvms.10-0573.
Lindsey JK: Growth curves. Statistical analysis of stochastic processes in time. Edited by: Gill R, Ripley BD, Ross S, Silverman BW, Stein M. 2004, Cambridge, UK: Cambridge university press, 268-284.
Nawata K, Matsubara M: Regression analysis for economical analysis. Statistical methods for the social and behavioral sciences (Basic statistics II). 1994, Tokyo, Japan: University of Tokyo press, 155-200. (in Japanese)
Broman KW, Sen Ś: A guide to QTL mapping with R/qtl. 2009, New York: Springer
Broman KW, Wu H, Sen Ś, Churchill GA: R/qtl: QTL mapping in experimental crosses. Bioinformatics. 2003, 19: 889-890. 10.1093/bioinformatics/btg112.
Lander E, Kruglyak L: Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995, 11: 241-247. 10.1038/ng1195-241.
Vogel H, Scherneck S, Kanzleiter T, Benz V, Kluge R, Stadion M, Kryvych S, Blüher M, Klöting N, Joost H-G, Schürmann A: Loss of function of Ifi202b by a microdeletion on chromosome 1 of C57BL/6J mice suppresses 11ß-hydroxysteroid dehydrogenase type 1 expression and development of obesity. Hum Mol Genet. 2012, 21: 3845-3857. 10.1093/hmg/dds213.
Scherneck S, Nestler M, Vogel H, Blüher M, Block MD, Diaz MB, Herzig S, Schulz N, Teichert M, Tischer S, Al-Hasani H, Kluge R, Schürmann A, Joost HG: Positional cloning of zinc finger domain transcription factor Zfp69, a candidate gene for obesity-associated diabetes contributed by mouse locus Nidd/SJL. PLoS Genet. 2009, 5: e1000541-10.1371/journal.pgen.1000541.
Yamauchi T, Kamon J, Waki H, Terauchi Y, Kubota N, Hara K, Mori Y, Ide T, Murakami K, Tsuboyama-Kasaoka N, Ezaki O, Akanuma Y, Gavrilova O, Vinson C, Reitman ML, Kagechika H, Shudo K, Yoda M, Nakano Y, Tobe K, Nagai R, Kimura S, Tomita M, Froguel P, Kadowaki T: The fat-derived hormone adiponectin reverses insulin resistance associated with both lipoatrophy and obesity. Nat Med. 2001, 7: 941-946. 10.1038/90984.
Yamauchi T, Kamon J, Minokoshi Y, Ito Y, Waki H, Uchida S, Yamashita S, Noda M, Kita S, Ueki K, Eto K, Akanuma Y, Froguel P, Foufelle F, Ferre P, Carling D, Kimura S, Nagai R, Kahn BB, Kadowaki T: Adiponectin stimulates glucose utilization and fatty-acid oxidation by activating AMP-activated kinase. Nat Med. 2008, 8: 1288-1295.
Kubota N, Terauchi Y, Yamauchi T, Kubota T, Moroi M, Matsui J, Eto K, Yamashita T, Kamon J, Satoh H, Yano W, Froguel P, Nagai R, Kimura S, Kadowaki T, Noda T: Disruption of adiponectin causes insulin resistance and neointimal formation. J Biol Chem. 2002, 277: 25863-25866. 10.1074/jbc.C200251200.
Nakajima Y, Imamura K, Onodera T, Goto N: Hydronephrosis in the inbred mouse strain DDD. Lab Anim. 1983, 17: 143-147. 10.1258/002367783780959538.
Goto N, Nakajima Y, Onodera T, Imamura K: Inheritance of hydronephrosis in the inbred mouse strain DDD. Lab Anim. 1984, 18: 22-25. 10.1258/002367784780864893.
Vogel H, Nestler M, Rüschendorf F, Block M-D, Tischer S, Kluge R, Schürmann A, Joost H-G, Scherneck S: Characterization of Nob3, a major quantitative trait locus for obesity and hyperglycemia on mouse chromosome 1. Physiol Genomics. 2009, 38: 226-232. 10.1152/physiolgenomics.00011.2009.
Plum L, Kluge R, Giesen K, Altmüller J, Ortlepp JR, Joost HG: Type 2 diabetes-like hyperglycemia in a backcross model of NZO and SJL mice. Diabetes. 2000, 49: 1590-1596. 10.2337/diabetes.49.9.1590.
Scherneck S, Vogel H, Nestler M, Kluge R, Schürmann A, Joost HG: Role of zinc finger transcription factor Zfp69 in body fat storage and diabetes susceptibility of mice. Results Prob Cell Differ. 2010, 52: 57-68.
Córdoba-Chacón J, Gahete MD, Pozo-Salas AI, Martínez-Fuentes AJ, de Lecea L, Gracia-Navarro F, Kineman RD, Castaño JP, Luque RM: Cortistatin is not a somatostatin analogue but stimulates prolactin release and inhibits GH and ACTH in a gender-dependent fashion: potential role of ghrelin. Endocrinology. 2011, 152: 4800-4812. 10.1210/en.2011-1542.
Semjonous NM, Sherlock M, Jeyasuria P, Parker KL, Walker EA, Stewart PM, Lavery GG: Hexose-6-phosphate dehydrogenase contributes to skeletal muscle homeostasis independent of 11ß-hydroxysteroid dehydrogenase type 1. Endocrinology. 2011, 152: 93-102. 10.1210/en.2010-0957.
Hummel KP, Coleman DL, Lane PW: The influence of genetic background on expression of mutations at the diabetes locus in the mouse. I. C57BL/KsJ and C57BL/6J strains. Biochem Genet. 1972, 7: 1-13. 10.1007/BF00487005.
Coleman DL, Hummel KP: The influence of genetic background on the expression of the obese (ob) gene in the mouse. Diabetologia. 1973, 9: 287-293. 10.1007/BF01221856.
Coleman DL: Obese and diabetes: two mutant genes causing diabetes-obesity syndromes in mice. Diabetologia. 1978, 14: 141-148. 10.1007/BF00429772.
Stoehr JP, Nadler ST, Schueler KL, Rabaglia ME, Yandell BS, Metz SA, Attie AD: Genetic obesity unmasks nonlinear interactions between murine type 2 diabetes susceptibility loci. Diabetes. 2000, 49: 1946-1954. 10.2337/diabetes.49.11.1946.
Qiu J, Ogus S, Mounzih K, Ewart-Toland A, Chehab FF: Leptin-deficient mice backcrossed to the BALB/cJ genetic background have reduced adiposity, enhanced fertility, normal body temperature, and severe diabetes. Endocrinology. 2001, 142: 3421-3425. 10.1210/en.142.8.3421.
Haluzik M, Colombo C, Gavrilova O, Chua S, Wolf N, Chen M, Stannard B, Dietz KR, Le Roith D, Reitman ML: Genetic background (C57BL/6J Versus FVB/N) strongly influences the severity of diabetes and insulin resistance in ob/ob mice. Endocrinology. 2004, 145: 3258-3264. 10.1210/en.2004-0219.
This study was supported in part by an institutional grant from NIAS.
The authors declare that they have no competing interests.
JS and KS conceived the study. JS conducted the experiments on mice. KS conducted statistical analysis for growth. JS conducted QTL mapping analysis. JS and KS wrote the manuscript. Both authors read and approved the final manuscript.
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Suto, Ji., Satou, K. Genetic background (DDD/Sgn versus C57BL/6J) strongly influences postnatal growth of male mice carrying the Ayallele at the agouti locus: identification of quantitative trait loci associated with diabetes and body weight loss. BMC Genet 14, 35 (2013). https://doi.org/10.1186/1471-2156-14-35
- Ay allele
- Body weight loss
- DDD mice
- Diabetes mellitus
- Growth analysis
- Quantitative trait locus (QTL)