- Research article
- Open Access
QTL analyses of temporal and intensity components of home-cage activity in KJR and C57BL/6J strains
BMC Genetics volume 10, Article number: 40 (2009)
A variety of mouse strains exhibit diversity in spontaneous activity consistent with an important genetic contribution. To date, many studies have defined spontaneous home-cage activity as total distance or total counts of activity within a test period. However, spontaneous activity is, in fact, a composite of elements of 'temporal' and 'intensity' that is similar to 'velocity'. Here, we report on quantitative trait loci for different components of spontaneous activity, an important step towards dissection of the underlying genetic mechanisms.
In the analysis of total home-cage activity (THA) after habituation in female mice, KJR strain exhibit higher activity than C57BL/6J (B6). In this study, THA was partitioned into two components: active time (AT) was an index of the 'temporal element' of THA, average activity during active time (AA) was an index of 'intensity'. Correlation analysis using B6xKJR F2 female mice indicated that AA is a major component of THA, whereas AA and AT were associated to a lesser degree. To explore the genetic basis of the activity differences, we conducted quantitative trait loci (QTL) analysis on data of THA and its components, AT and AA. Three significant QTL affecting variation of different components of home cage activity were identified, two linked QTL Hylaq1 and Hylaq2 on Chr 2, and Hylaq3 on Chr 10. Chromosomal positions of these QTL were previously implicated in locomotor activity (Chr 2) or open-field ambulation (Chr 10). The results indicated that Hylaq1 influences AT, Hylaq2, AA, while Hylaq3 is associated with both AA and AT.
Through this study, we found that variation in total home cage activity over a 3 day period is affected by variation in active time and intensity of activity. The latter two variables are distinct components of home cage activity with only partially overlapping genetic architecture.
Spontaneous activity is a key feature of an animal's interaction with its environment reflecting a variety of metabolic, physiological and neurological processes. It has been reported that many laboratory strains of rodents exhibit variation in locomotor activity that are influenced by genetic factors. For example, Plomin et al. identified quantitative trait loci (QTLs) related to locomotor activity in the open field using Recombinant inbred mouse strains (BXD) . Several other genetic studies focused on differences of the open-field activity between various kind of mouse strains and found many QTLs [2–7]. In rats, Hendley et al. established a Wistar-Kyoto hyperactive (WKHA) strain that exhibits increased spontaneous activity in a novel environment . A subsequent genetic study clarified QTL related to open-field activity in WKHA .
However, ambulation or locomotion in open-field often reflects motivational and situational influences [10–13]. From this point of view, measuring home-cage activity is more suitable for estimating spontaneous or general activity, but there are not many reports on QTL related to spontaneous activity in a home cage . Koyner et al. found QTL related to basal activity on Chr 1, 5 and 9 using an arena apparatus covered with standard laboratory bedding that mimicked the home-cage environment . By conducting genetic analysis using similar apparatus, QTLs related to basal activity were identified on Chr 1, 9 and 19 ; Chr 1, 2 and 6 ; Chr 4, 8, 11, 14, 18 and X ; and Chr 1 . Recently, QTL mapping was conducted using automated home-cage measuring apparatus and mapped a locus related to spontaneous activity on Chr 1 [19, 20].
Previously, our laboratory conducted multi-phenotype behavioral characterization using a series of inbred strains derived from wild mice in addition to commonly used laboratory strains . The results showed great diversity among strains in terms of the behavioral patterns, including spontaneous locomotor activity in the home cage. In particular, the activity of the KJR/Ms (KJR) strain was significantly higher than that of BLG2 and C57BL/6J (B6). Linkage analysis in the KJR and BLG2 backcross showed that two loci, Loco1 on Chr 3 and Loco2 on Chr17 influenced spontaneous locomotor activity in the home-cage . However, the actual level of spontaneous locomotor activity during a defined period of time can be achieved by either short bursts of rapid movement or by steady, slow movement throughout the period, furthermore, the frequency of the bursts of activity may also vary. In fact, in most instances both 'temporal' and 'intensity' elements contribute to total activity to varying degrees. Importantly, each of those elements is likely to reflect the function distinct biological mechanisms and recent reports suggested that the genetic variation can differentially influence temporal and velocity (intensity) phenotypes . For instance, the pattern of the bursts of activity is determined by CNS mechanisms influencing sleep and activity, whereas the intensity of activity might be an outcome of neuromuscular function. Therefore, in the present paper we attempted extract additional information about the mechanism contributing to spontaneous home cage activity by partitioning it into two components.
The KJR strain is derived from wild mice captured in Kojuri, Korea , and belongs to the musculus subspecies group that is widely distributed from east Europe to Asia. KJR mice have retained some aspects of the wild phenotype, e.g. quick movement, pronounced inter-male aggressive behavior and high emotionality. In particular, KJR mice move quickly for long periods, resulting in high counts in the three-day measurement of spontaneous locomotor activity .
B6 is derived from European fancy mice and belongs to the domesticus subspecies group that is distributed in West Europe [23, 24]. Compared to KJR, B6 shows typical features of laboratory mice, e.g. slow movement and low-impulsive behavior. In addition, B6 showed intermediate level total home-cage activity among the tested strains, but this was significantly lower than that of KJR . Thus, KJR and B6 are hypothesized to have different genetic mechanisms involved in spontaneous activity in the home cage.
In the present study we aimed to identify the genetic architecture underlying temporal and intensity components of home cage activity using phenotypically divergent inbred strain.
Mouse strains and maintenance
C57BL/6J (B6) and KJR/Ms (KJR) inbred strains were maintained in the animal facility at the National Institute of Genetics (NIG), Mishima, Japan. KJR was established as an inbred strain after 20 generations of brother-sister mating . For genetic mapping, F2 populations (B6xKJR F2) were generated by an intercross of the F1 mice (B6xKJR F1). Based on the previous report in which a significant difference in home-cage activity was observed between B6 and KJR in females , 274 female B6xKJR F2 mice aged between 8 and 12 weeks were generated and used to measure activities in the home-cage. All mice were maintained at NIG on a 12 h/12 h light/dark cycle with lights coming on at 8:00 a.m. Temperature was maintained at 23 ± 2°C with humidity at 50 ± 10%. Mice were fed a pelleted diet (CE-2; CLEA Japan Inc, Tokyo, Japan) ad libitum, and autoclaved tap water. Mice were maintained according to NIG guidelines, and all procedures were carried out with approval (No. 18-18 and 19-6) from our institutional animal care and use committee.
Measurement and analysis of spontaneous activity in home cage
The spontaneous activity in the habituated home cage was measured according to the method described previously . The spontaneous home-cage activity was assessed for individual mice with an infrared sensor, AB-system 24 (Neuroscience Co. Ltd., Tokyo, Japan) for a 4-day period, with the first day used for habituation. The photo beam counts were collected for each minute from 08:00 a.m. of the second day to 08:00 a.m. of the fifth day for each mouse. Total spontaneous home-cage activity (THA) was the index of total activity in the home cage and calculated as the sum of total beam counts across the three days.
Calculation of heritability
Broad-sense heritability (H2) is the fraction of the total phenotypic variance (VT) that is due to genetic differences among individuals in a population (VG) and calculated as follows;
In this study, VT was calculated as a variance of B6xKJR F2 population, and environmental variance (VE) was the variance among the B6xKJR F1 population (N = 11). Thus, VG was the difference between VT and VE.
Genotyping using microsatellite polymorphisms
Genomic DNA of each mouse was isolated from the tail by using an automatic nucleic acid isolation system, NA-2000 (KURABO, Osaka, Japan). A total 135 polymorphic microsatellite markers were chosen for genome-wide scanning of 274 B6xKJR F2 progeny. Microsatellite markers were spaced between 5 to 20 cM, and determined by the method as described previously . Microsatellite markers used for B6xKJR F2 progeny: D1Mit296, D1Mit318, D1Mit414, D1Mit132, D1Mit365, D1Mit309, D1Mit16, D2Mit2, D2Mit120, D2Mit203, D2Mit8, D2Mit9, D2Mit126, D2Mit30, D2Mit208, D2Mit423, D2Mit22, D2Mit55, D2Mit29, D2Mit265, D2Mit200, D3Mit149, D3Mit4, D3Mit51, D3Mit216, D3Mit147, D3Mit163, D4Mit235, D4Mit236, D4Mit288, D4Mit153, D4Mit12, D4Mit127, D4Mit254, D5Mit48, D5Mit4, D5Mit6, D5Mit403, D5Mit242, D5Mit51, D6Mit83, D6Mit316, D6Mit102, D6Mit287, D6Mit25, D7Mit191, D7Mit155, D7Mit69, D7Mit194, D7Mit31, D7Mit37, D7Mit66, D7Mit9, D7Mit108, D7Mit12, D8Mit1, D8Mit293, D8Mit69, D8Mit240, D8Mit242, D8Mit200, D8Mit13, D9Mit251, D9Mit23, D9Mit260, D9Mit10, D9Mit182, D9Mit24, D9Mit279, D9Mit121, D10Mit106, D10Mit5, D10Mit15, D10Mit186, D10Mit117, D10Mit70, D10Mit150, D10Mit73, D10Mit295, D10Mit180, D10Mit237, D10Mit145, D10Mit103, D11Mit23, D11Mit28, D11Mit327, D11Mit145, D11Mit214, D12Mit37, D12Mit147, D12Mit5, D12Mit118, D13Mit14, D13Mit88, D13Mit126, D13Mit262, D13Mit35, D14Mit2, D14Mit233, D14Mit102, D14Mit160, D14Mit265, D14Mit107, D15Mit226, D15Mit267, D15Mit111, D15Mit5, D15Mit121, D15Mit156, D16Mit34, D16Mit3, D16Mit65, D16Mit203, D17Mit164, D17Mit11, D17Mit36, D17Mit139, D17Mit129, D18Mit19, D18Mit68, D18Mit14, D18Mit35, D18Mit123, D18Mit2, D18Mit186, D19Mit109, D19Mit13, D19Mit1, D19Mit71, DXMit55, DXMit166, DXMit114, DXMit172, DXMit153, DXMit186, Genomic DNA prepared from the tail of B6xKJR F2 mice was amplified by polymerase chain reaction(PCR) with primer sets for microsatellite markers and analyzed by agarose gel electrophoresis with 4% agarose (3:1 Nusieve:Seakem agarose, FMC Bioproducts, Rockland, ME, USA) in 1 × TAE buffer. The bands visualized by ethidium staining from B6xKJR F2 mice were analyzed for length polymorphisms with reference to the polymorphisms of each marker between B6 and KJR.
Phenotypic and genetic data for 274 B6xKJR F2 progeny mice were analyzed by interval mapping (IM) and multiple regression analysis with R/qtl and J/qtl  to detect loci associated with three components of spontaneous home-cage activity. To explore possible pleiotropic effects on the home-cage activity phenotypes, QTL analysis of each trait was also conducted with a correlated phenotype as a covariate. For each analysis, genome-wide thresholds for suggestive (P < 0.63), significant (P < 0.05) and highly significant (P < 0.001) QTL were determined by 1000 permutations.
Composite interval mapping performed with QTL Cartographer
Composite interval mapping (CIM, [27, 28]) was performed with QTL Cartographer ver. 2.0  to study whether multiple QTL exist on the same chromosome where significant QTL were found in the interval mapping analysis. Five markers determined by a forward regression model were used as a background control in a CIM standard model. The window size was 10 cM. To obtain a more reliable threshold value, and to confirm the significance of detected QTLs, one thousand permutation tests (P < 0.05) were performed with QTL Cartographer for each trait. Furthermore, the additive effect (EA) and dominance effect (ED) at the peak of each significant QTL were also calculated by QTL Cartographer to study the effective size of each detected QTLs. Phenotypic variance (VP) explained by each QTL was calculated using these values as follows:
Then, the percent contribution of each locus was calculated from the phenotypic variance at the peak of each Hylaq locus (VP) divided by total phenotypic variance in B6xKJR F2 (VT).
Structural equation model (SEM)
In order to characterize the structure of genetic system on spontaneous activity, we applied SEM analysis [30, 31] to our data. SEM is a statistical method for testing an assumed causal relationship among variables, and usually represents the relationship as a direct path graph. Thus, we can easily test a model of the influence of the detected QTLs to the phenotype through this analysis. SEM can graphically illustrate the network among multiple genetic and phenotypic factors for spontaneous activity. We conducted SEM analysis by a method reported previously  using AMOS 7.0 . In order to conduct SEM analysis, we used QTLs identified by IM for AT and AA, and the identified QTLs by IM with covariates for the phenotypes. Then the path model was tested for the genetic model of QTLs for two quantitative traits, AT and AA.
An initial path model was defined based on an instruction by Li et al.  and the model was refined by following two steps.
First step: Path was deleted when the t-test value was not significantly different from zero or path coefficient with absolute value was lower than 0.05. In this case, change of the chi-square goodness of fit statistic should be less than 3.84 to indicate insignificance in the likelihood ratio test. If the obtained model meets following six standards , then the model was considered as a final path model. (1) it should be identified or overidentified with at least 1 residual df; (2) the goodness-fit test should be P > 0.05; (3) the largest standardized residual should not exceed 2.0 in absolute value; (4) individual path coefficients should be significantly different from zero based on the t-test; (5) standardized path coefficients should not be trivial (absolute values exceed 0.05); (6) a substantial proportion of the phenotypic variance of the endogenous variables should be explained by the model. If any of these standards were not fit to the model, we further modified as described in the Second step.
Second step: Add a path which causes a biggest change in p-value for the chi-square goodness of fit test and a significant change in the likelihood ratio test. Then, the modified model was tested as described in the First step.
Data analysis was performed with the StatView software package (SAS Institute Inc., Cary, NC, USA) and SPSS software package (SPSS Inc., Chicago, USA). Analysis of variance (ANOVA) was applied to determine the effect of strain or genotype. Post hoc analysis utilized the Fisher's Protected Least Significant difference (PLSD) test. The Kolmogorov-Smirnov (KS) test  was used to test the normality of the distribution on the measurements. In the KS test, when KS value exceeded 0.05, normal distribution model will not be denied.
Mapping information of identified QTLs, Hylaq1, Hylaq2 and Hylaq3 have been deposited in the Mouse Genome Database .
Spontaneous home-cage activity
Distributions in the parental strains and B6xKJR F1 for THA are shown in Figure 1(A). The groups were too small to conduct a meaningful assessment of the distribution but on the basis of the distributions of the F2 data (see below) we used parametric statistics for these analyses. One-way ANOVA indicated a significant difference among mouse groups in total home-cage activity (THA), F (2,28) = 80.3, P < 0.0001 (Table 1). KJR and B6xKJR F1 groups had significantly greater THA than B6 (post hoc analysis, P < 0.0001 in both cases). There was no significant difference between KJR and B6xKJR F1 groups.
THA was divided into two components, active time (AT) and average activity (AA). AT, an index of 'temporal component' was calculated as total minutes that exhibited more than one count within a one-minute interval. Hence, AT was estimated as the approximate duration of movement. Average activity (AA), an index of 'intensity' was calculated as follows:
The AA reflected average amount of locomotion over one minute of active time.
Distributions of the parental strains and B6xKJR F1 for AT and AA are shown in Figure 1B and 1C. One-way ANOVA found a significant difference among different groups of mice in AT, F (2, 28) = 34.3, P < 0.0001 (Table 1). KJR showed 13% higher AT value than B6 (post hoc analysis, P < 0.01). The AT of the B6xKJR F1 population was significantly greater than that of B6 and KJR (post hoc analysis, P < 0.0001).
In AA, one-way ANOVA indicated significant mouse group difference, F (2, 28) = 76.2, P < 0.0001 (Table 1). KJR exhibited more than 2-fold greater AA than B6 (post hoc analysis, P < 0.0001). The AA of B6xKJR F1 was intermediate between KJR and B6: AA in B6xKJR F1 was significantly higher than that of B6 (P < 0.0001) and lower than that of KJR (P < 0.01).
The relationship among three traits associated with home-cage activity
The Kolmogorov-Smirnov (KS) values (Figure 1D, E, F) were consistent with normality for all three indices (THA, AT and AA) and hence we used parametric statistics. In order to test the relationship between the three variables in the B6xKJR F2 we conducted Pearson's correlation test (Additional file 1). THA and AT were moderately associated (r = 0.686, P < 0.0001), whereas THA and AA showed a high correlation (r = 0.935, P < 0.0001). And AA and AT were modestly correlated (r = 0.401, P < 0.0001). Thus the outcome of analysis suggested that mechanisms underlying variation of the AA and THA variables have a greater degree of commonality than those underlying variation between the AT and THA.
Broad-sense heritability values (H2) in THA, AT, and AA were 0.62, 0.53 and 0.72, respectively (Table 1). In order to identify the genetic factors related to these traits, we conducted QTL analyses. Interval mapping (IM) analyses detected two highly significant QTLs (P < 0.001) on Chr 2 and 10 for THA (Figure 2A, black lines), one highly significant QTL on Chr 10 for AA (Figure 2B, black lines), and one highly significant QTLs on Chr 2 and a significant QTL on Chr 10 for AT (Figure 2C, black line). No significant epistatic interaction between markers was detected in an analysis using R/qtl (data not shown).
Since correlation analyses indicated that three traits of spontaneous activity were interrelated with each other, to assess the nature of their relationship we conducted QTL analyses on each trait of spontaneous activity with two other traits as covariates (Figure 2A–C). The results suggested pleiotropic effects of the QTL on Chr 2 (on THA and AT) and on Chr 10 (on THA and AA).
Mice exhibited a remarkable difference of activity between the light and dark phases (Additional file 2). We divided home-cage activity data into two periods, light phase activity and dark phase activity, and conducted QTL analyses to search for loci related to home-cage activities in these two phases. No significant loci were identified in the light phase (Additional file 3), whereas, in the dark phase, we obtained similar results of QTL as that of whole periods (Additional file 4). In order to investigate effect of day of the experiment, we also conducted IM on each of three days activity data. However, we did not observe a clear difference in the genetic architecture on any day (Additional file 5).
In order to investigate QTLs on Chr 2 and 10 in more detail, we applied Composite interval mapping (CIM) to these chromosomes. Permutation tests (P < 0.05) showed that the threshold values of significant LOD scores were 3.6, 3.7 and 3.6, for THA, AT and AA, respectively. The CIM detected two significant LOD peaks associated with THA, AT, and AA on Chr 2 (Figure 3A, Table 2). Two linked QTL were also implied by a multi-trait analysis on the correlated AT and AA phenotypes (Additional file 6). In the middle region on Chr 2, significant peaks involved in THA, AT and AA overlapped each other and were located between D2Mit126 and D2Mit423. We designated this locus hyperlocomotor activity related QTL (Hylaq1). In the distal side of the Hylaq1 on Chr 2, significant peaks associated with THA, AT and AA were located between D2Mit22 and D2Mit29. This locus was designated Hylaq2. In the telomeric region on Chr 10, a broad locus with several peaks associated with THA and AA was detected between D10Mit73 and D10Mit180. This locus was designated Hylaq3, mainly associated with THA and AA (Figure 3B, Table 2). Scores of effect size showed a relatively high contribution to the phenotypic variance (Table 2): Hylaq1 and Hylaq2 accounted for 11.9 and 15.2%, respectively, on AT.
In order to explore the relationship among the QTL affecting different activity components, AT and AA, and also the relationship between the two components themselves we conducted SEM analysis based on the results of IM with covariates (Figure 4). The results (for details see Methods and Additional file 7) indicated that both Hylaq1 and Hylaq3 influence AT and both Hylaq2 and Hylaq3 associate with AA, furthermore, it showed that variation in AT was causative to that in AA.
In this study, we investigated the difference in spontaneous locomotor activity in terms of total home-cage activity, by partitioning it into temporal and velocity elements of the behavior, between the KJR and B6 strains. Pearson correlation analysis between AT and AA showed a low score (r = 0.400), indicating that these two measurements reflect largely distinct biological processes, AT is temporal (how much time from the total period of 72 hours animals were active) whereas AA is the average amount of activity within a 1 minute period. A high correlation between AA and a collective total home cage activity, THA, (0.935) indicated that the intensity of activity within 1 min time period predicted the total activity across 3 days. Partitioning of THA into AA and AT provided information about the effects of the genetic variation on the processes contributing to the overall spontaneous activity. This is consistent with a previous study which also demonstrated that a 'temporal element' and 'velocity' in a home-cage are controlled by different genetic bases .
QTL analysis identified three loci, Hylaq1, Hylaq2 and Hylaq3, associated with spontaneous home-cage activity. These QTLs, especially, Hylaq1 and Hylaq3 have a relatively large effective size (11.9 and 15.2% of phenotypic variance, respectively; Table 2), which exceed generally found effects in behavioral traits , and will facilitate fine mapping of these loci. By searching the MGI database , a number of locomotor activity-related QTLs were found in the region between D2Mit126 and D2Mit29 (Table 3, [6, 7, 17, 37–41]), these markers are located at just outside of two LOD support interval (90% confidence interval) below the peak of Hylaq1 and Hylaq2. Because the genetic positions were not precisely comparable among different experiments, we only list the following QTLs as possibly having genetic communality with Hylaq1, Hylaq2 and Hylaq3. Five QTLs, Actre2, Etohr, Cplaq7, Actre3 and Actre4, are located around the region of Hylaq1 and four QTLs, Rrodp2, Slms2, Nilac3 and Dloc1 which are in close proximity to the Hylaq2 loci on Chr 2. Concerning Hylaq3, there are no QTL directly associated with spontaneous home-cage activity at the same locus on Chr 10 in the database. However, one QTL, Exq1, associated with open-field ambulation was reported in the region just distal side of the two LOD support interval markers, D10Mit73 and D10Mit103, on Chr 10 [3, 42].
In this study, we found that Hylaq3 influences both the temporal and intensity elements of spontaneous activity (AT and AA) in a pleiotropic manner. In the context of the phenotype-specific effects of the Hylaq1 and Hylaq2, this observation suggests an overlap of a certain degree between the mechanisms underlying temporal- and intensity-related phenotypes of spontaneous home cage activity. However, further research is required to discriminate between the scenarios of the pleiotropic effect of the same gene versus the influence of closely linked genes on AT and AA.
In the present study the Hylaq1, Hylaq2 and Hylaq3 loci were identified in the analysis of the composite THA phenotype, thus partitioning it into the AT and AA components did not identify additional loci. However, this approach provided auxiliary information about the nature of variation in THA, e.g., longer cumulative period of activity vs greater intensity, which might be important for nomination of the candidate genes in the fine mapping stage the effort.
In the present study, we used only females to examine home-cage activity, because the previous study showed clear difference of activity of females in the parental strains. However, it is possible that we could find different QTL in males. This attempt to find sex specific QTL on behaviour will be of considerable value.
The present study clarified the genetic basis for different components of spontaneous activity. The identified QTLs had a relatively large effect size and are amenable for subsequent fine mapping studies. This result support the potential of wild derived strains, such as KJR, in understanding the mechanism of genetic regulation of behavioural phenotypes.
Plomin R, McClearn GE, Gora-Maslak G, Neiderhiser JM: Use of recombinant inbred strains to detect quantitative trait loci associated with behavior. Behav Genet. 1991, 21: 99-116. 10.1007/BF01066330.
Flint J, Corley R, DeFries JC, Fulker DW, Gray JA, Miller S, Collins AC: A simple genetic basis for a complex psychological trait in laboratory mice. Science. 1995, 269: 1432-5. 10.1126/science.7660127.
Gershenfeld HK, Neumann PE, Mathis C, Crawley JN, Li X, Paul SM: Mapping quantitative trait loci for open-field behavior in mice. Behav Genet. 1997, 27: 201-210. 10.1023/A:1025653812535.
Turri MG, Henderson ND, DeFries JC, Flint J: Quantitative trait locus mapping in laboratory mice derived from a replicated selection experiment for open-field activity. Genetics. 2001, 158: 1217-26.
Turri MG, Datta SR, DeFries J, Henderson ND, Flint J: QTL analysis identifies multiple behavioral dimensions in ethological tests of anxiety in laboratory mice. Curr Biol. 2001, 11: 725-734. 10.1016/S0960-9822(01)00206-8.
Kelly MA, Low MJ, Phillips TJ, Wakeland EK, Yanagisawa M: The mapping of quantitative trait loci underlying strain differences in locomotor activity between 129S6 and B6 mice. Mamm Genome. 2003, 14: 692-702. 10.1007/s00335-003-2273-0.
Gill KJ, Boyle AE: Genetic basis for the psychostimulant effects of nicotine: a quantitative trait locus analysis in AcB/BcA recombinant congenic mice. Genes Brain Behav. 2005, 4: 401-411. 10.1111/j.1601-183X.2005.00116.x.
Hendley ED, Ohlsson WG: Two new inbred rat strains derived from SHR: WKHA, hyperactive, and WKHT, hypertensive, rats. Am J Physiol. 1991, 261: H583-589.
Moisan MP, Courvoisier H, Bihoreau MT, Gauguier D, Hendley ED, Lathrop M, James MR, Mormede P: A major quantitative trait locus influences hyperactivity in the WKHA rat. Nat Genet. 1996, 14: 471-473. 10.1038/ng1296-471.
Blizard DA, Takahashi A, Galsworthy MJ, Martin B, Koide T: Test Standardization in behavioural neuroscience: a response to Stanford. J Psychopharmacology. 2007, 21: 136-139. 10.1177/0269881107074513.
Rodgers RJ: More haste, considerably less speed. J Psychopharmacol. 2007, 21: 141-143. 10.1177/0269881107074493.
Stanford SC: The Open Field Test: reinventing the wheel. J Psychopharmacol. 2007, 21: 134-135. 10.1177/0269881107073199.
Takahashi A, Kato K, Makino J, Shiroishi T, Koide T: Multivariate analysis of temporal descriptions of open-field behavior in wild-derived mouse strains. Behav Genet. 2006, 36: 763-764. 10.1007/s10519-005-9038-3.
Flint J: Analysis of quantitative trait loci that influence animal behavior. J Neurobiol. 2003, 54: 46-77. 10.1002/neu.10161.
Koyner J, Demarest K, McCaughran JJr, Cipp L, Hitzemann R: Identification and time dependence of quantitative trait loci for basal locomotor activity in the BXD recombinant inbred series and a B6D2 F2 intercross. Behav Genet. 2000, 30: 159-170. 10.1023/A:1001963906258.
Hitzemann R, Demarest K, Koyner J, Cipp L, Patel N, Rasmussen E, McCaughran J: Effect of genetic cross on the detection of quantitative trait loci and a novel approach to mapping QTLs. Pharmacol Biochem Behav. 2000, 67: 767-72. 10.1016/S0091-3057(00)00421-4.
Demarest K, Koyner J, McCaughran J, Cipp L, Hitzemann R: Further characterization and high-resolution mapping of quantitative trait loci for ethanol-induced locomotor activity. Behav Genet. 2001, 31: 79-91. 10.1023/A:1010261909853.
Hitzemann R, Malmanger B, Reed C, Lawler M, Hitzemann B, Coulombe S, Buck K, Rademacher B, Walter N, Polyakov Y, Sikela J, Gensler B, Burgers S, Williams RW, Manly K, Flint J, Talbot C: A strategy for the integration of QTL, gene expression, and sequence analyses. Mamm Genome. 2003, 14: 733-47. 10.1007/s00335-003-2277-9.
de Visser L, Bos van den R, Kuurman WW, Kas MJH, Spruijt BM: Novel approach to the behavioural characterization of inbred mice: automated home cage observations. Genes Brain Behav. 2006, 5: 458-466. 10.1111/j.1601-183X.2005.00181.x.
Kas MJ, de Mooij-van Malsen A, de Krom M, van Gassen KL, van Lith HA, Olivier B, Oppelaar H, Hendriks J, de Wit M, Groot Koerkamp MJ, Holstege FC, van Oost BA, de Graan PN: High resolution genetic mapping of mammalian motor activity levels in mice. Genes Brain Behav. 2008, 8: 13-22. 10.1111/j.1601-183X.2008.00435.x.
Koide T, Moriwaki K, Ikeda K, Niki H, Shiroishi T: Multi-phenotype behavioral characterization of inbred strains derived from wild stocks of Mus musculus. Mamm Genome. 2000, 11: 664-670. 10.1007/s003350010129.
Furuse T, Takano-Shimizu T, Moriwaki K, Shiroishi T, Koide T: QTL analyses of spontaneous activity by using mouse strains from Mishima battery. Mamm Genome. 2002, 13: 411-415. 10.1007/s00335-002-2168-5.
Bonhomme , Guénet : The laboratory mouse and its wild relatives. Genetic variants and strains of the laboratory mouse. Edited by: Lyon MF, Rastan S, Brown SDN. 1996, Oxford, Oxford University Press, 1577-1596.
Moriwaki K, Shiroishi T, Yonekawa H: Genetics in wild mice. 1994, Tokyo/Basel, Japan Scientific Societies Press/Karger
Koide T, Moriwaki K, Uchida K, Mita A, Sagai T, Yonekawa H, Katoh H, Miyashita N, Tsuchiya K, Nielsen TJ, Shiroishi T: A new inbred strain JF1 established from Japanese fancy mouse carrying the classic piebald allele. Mamm Genome. 1998, 9: 15-19. 10.1007/s003359900672.
Broman KW, Wu H, Sen S, Churchill GA: R/qtl: QTL mapping in experimental crosses. Bioinformatics. 2003, 19: 889-890. 10.1093/bioinformatics/btg112.
Zeng ZB: Theoretical basis for separation of multiple linked gene effects in mapping quantitative trait loci. Proc Natl Acad Sci USA. 1993, 90: 10972-10976. 10.1073/pnas.90.23.10972.
Zeng ZB: Precision mapping of quantitative trait loci. Genetics. 1994, 136: 1457-1468.
Basten CJ, Weir BS, Zeng ZB: QTL Cartographer. A reference manual and tutorial for QTL mapping. 1999, Raleigh, NC, Department of Statics, North Carolina State University
Bollen KA: Structural Equations with Latent Variables. 1989, New York, Wiley-Interscience
Meyers LS, Gamst GC, Guarino AJ: Applied Multivariate Research: Design and Interpretation. 2006, Thousand Oaks, Sage Publications
Li R, Tsaih SW, Shockley K, Stylianou IM, Wergedal J, Paigen B, Churchill GA: Structural model analysis of multiple quantitative traits. PLoS Genet. 2006, 2: 1046-1057.
Arbuckle JL: Amos 7.0 User's Guide. 2006, Pennsylvania, Amos Development Corporation
Chakravarti , Laha , Roy : Handbook of Methods of Applied Statistics. 1967, New York, John Wiley and Sons, I:
Mouse Genome Informatics. [http://www.informatics.jax.org/searches/allele_form.shtml]
Valdar W, Solberg LC, Gauguier D, et al: Genome-wide genetic association of complex traits in heterogeneous stock mice. Nat Genet. 2006, 38: 879-887. 10.1038/ng1840.
Hitzemann R, Cipp L, Demarest K, Mahjubi E, McCaughran J: Genetics of ethanol-induced locomotor activation: detection of QTLs in a C57BL/6J × DBA/2J F2 intercross. Mamm Genome. 1998, 9: 956-962. 10.1007/s003359900906.
Demarest K, McCaughran J, Mahjubi E, Cipp L, Hitzemann R: Identification of an acute ethanol response quantitative trait locus on mouse chromosome 2. J Neurosci. 1999, 19: 549-61.
Hofstetter JR, Mayeda AR, Possidente B, Nurnberger JI: Quantitative trait loci (QTL) for circadian rhythms of locomotor activity in mice. Behav Genet. 1995, 25: 545-556. 10.1007/BF02327578.
Hofstetter JR, Trofatter JA, Kernek KL, Nurnberger JI, Mayeda AR: New quantitative trait loci for the genetic variance in circadian period of locomotor activity between inbred strains of mice. J Biol Rhythms. 2003, 18: 450-62. 10.1177/0748730403259468.
Palmer AA, Lessov-Schlaggar CN, Ponder CA, McKinnon CS, Phillips TJ: Sensitivity to the locomotor-stimulant effects of ethanol and allopregnanolone: a quantitative trait locus study of common genetic influence. Genes Brain Behav. 2006, 5: 506-17. 10.1111/j.1601-183X.2005.00198.x.
Gershenfeld HK, Neumann PE, Li X, St Jean PL, Paul SM: Mapping quantitative trait loci for seizure response to a GABAA receptor inverse agonist in mice. J Neurosci. 1999, 19: 3731-8.
We are grateful to T. Shiroishi for valuable advice throughout this work, to K. Moriwaki for his considerable work in establishing the KJR strain, and to G.P. Vogler for advice on structural equation modeling. We thank all members of the Mouse Genomics Resource Laboratory at NIG for rearing the mice and for supporting this study. This study was supported by KAKENHI (Grant-in-Aid for Scientific Research) on Priority Areas "Comparative Genomics" from the Ministry of Education, Culture, Sports, Science and Technology (TK), and Research Organization of Information and Systems, Transdisciplinary Research Integration Center (JU, TS, SK, TK). This study has contribution number 2509 from the NIG.
JU collected data for behaviors and genotypes, analyzed the data, and made a draft of the manuscript. AN participated in the behavioral analyses. AL and DAB conducted QTL analysis with covariates. TS and SK conducted SEM analysis. TK supervised the project. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 2: Distribution of activity scores in B6xKJR F2. Distribution of THA, AT and AA in whole period (white bars) and in dark period (black bars) in B6xKJR F2. (PDF 30 KB)
Additional file 3: Interval mapping on activity data of the light phase. No significant QTL was found on activity data of the light phase. (PDF 169 KB)
Additional file 4: Results of interval mapping on activity data of the dark phase. QTLs found on activity data in dark phase were similar to that of whole period. (PDF 137 KB)
Additional file 5: Results of interval mapping on each day's data. Results of QTL analysis on each day's activity data showed similar pattern as entire three days period. (PDF 146 KB)
Additional file 6: Multiple traits analysis using AT and AA. Multiple traits analysis also supports that there are at least two loci, Hylaq1 and Hylaq2, located close to each other on Chr 2. (PDF 55 KB)
Additional file 7: Structural Equation Modeling (SEM) analysis. The path model indicated that Hylaq1 influences AT, Hylaq2, AA, while Hylaq3 is associated with both AA and AT. (PDF 17 KB)
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Umemori, J., Nishi, A., Lionikas, A. et al. QTL analyses of temporal and intensity components of home-cage activity in KJR and C57BL/6J strains. BMC Genet 10, 40 (2009). https://doi.org/10.1186/1471-2156-10-40
- Quantitative Trait Locus
- Active Time
- Spontaneous Activity
- Quantitative Trait Locus Analysis
- Composite Interval Mapping