Abstract
BackgroundWe previously established a congenic mouse strain with TALLYHO/Jng (TH) donor segment on chromosome 6 in a C57BL/6 (B6) background that harbors an obesity quantitative trait locus, tabw2. The B6.TH-tabw2 congenic mice developed increased adiposity that became exacerbated upon feeding a high fat-high sucrose (HFS) diet. To fine map the tabw2, in this study we generated and characterized subcongenic lines with smaller TH donor segments.ResultsWe fixed four subcongenic lines, with maximum size of donor segment retained in the lines ranging from 10.8 – 92.5 Mb. For mapping, all the subcongenic mice, along with B6.TH-tabw2 congenic and B6-homozygous control mice were fed either chow or HFS diets, and their post-mortem fat pads were weighed. Mice were also characterized for energy expenditure, respiratory exchange ratio, locomotor activity, and food intake. As previously reported, B6.TH-tabw2 congenic mice showed a significantly larger fat mass than controls on both diets. On chow, a subcongenic line retaining the distal region of the TH donor congenic interval exhibited significantly larger fat mass than B6-homozygous controls, and comparable that to B6.TH-tabw2 congenic mice. Two nested subcongenic lines within that region suggested that the effect of tabw2 on obesity could be attributed to at least two subloci. On HFS diets, on the other hand, all the subcongenic mice had significantly larger fat mass than controls without genotype differences, but none of them had fat mass as large as the original congenic mice. This possibly implicates that further genetic complexity involves in the effect of tabw2 on diet-induced obesity. Significantly reduced locomotor activity was exhibited in B6.TH-tabw2 congenic and subcongenic mice compared to controls when animals were fed HFS diets. B6.TH-tabw2 congenic mice, but not subcongenic mice, also had significantly increased food intake on HFS diets.ConclusionsIt appears that at least two subloci explaining the tabw2 effect under chow feeding map to the distal region of the congenic interval, whereas the diet-induced obesity mediated by tabw2 is attributed to more complex genetic mechanism.
Highlights
We previously established a congenic mouse strain with TALLYHO/Jng (TH) donor segment on chromosome 6 in a C57BL/6 (B6) background that harbors an obesity quantitative trait locus, tabw2
Unlike conventional linkage mapping, such as with F2 cross, multiple mice with the same recombination can be analyzed from subcongenic lines, resulting in more accurate estimation of the phenotype conferred by the quantitative trait locus (QTL)
Generation of subcongenic lines of mice for tabw2 QTL on chromosome 6 To fine map the tabw2 QTL, subcongenic lines of mice with different segments of the TH donor congenic interval were generated from B6.TH-tabw2 congenic mice (Figure 1)
Summary
We previously established a congenic mouse strain with TALLYHO/Jng (TH) donor segment on chromosome 6 in a C57BL/6 (B6) background that harbors an obesity quantitative trait locus, tabw. We have established a congenic mouse strain that harbors a TH-derived chromosome 6 genomic segment containing an obesity quantitative trait locus (QTL), tabw (TALLYHO associated body weight 2), on a B6 background [11]. This B6.TH-tabw congenic strain develops increased adiposity that becomes exacerbated upon feeding high fat-high sucrose (HFS) diets. This subcongenic approach has been successfully used for refining the location of QTLs and identification of susceptibility genes for diabetes and obesity [12,13,14]
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