Mouse loci associated with life span exhibit sex-specific and epistatic effects.
نویسندگان
چکیده
We have looked for genetic predictors of life span in a sibship of mice created as a four-way cross among inbred grandparental strains BALB/cJ, C57BL/6J, C3H/HeJ, and DBA/2J. To minimize the potential confounding effects of loci that influence early-life illnesses only, we conducted two analyses: one involving all the mice, and the other using a data set from which the first 20% of the deaths were excluded. The two strongest associations reach experimentwise significance levels (p <.01) when tested on the 80% of the mice with the longest life spans. Surprisingly, three of the four strongest associations showed sex-specific effects, with an influence on life span of either male or female mice, but not both. Epistatic interactions among the loci were also identified. The life-span effect of a locus on chromosome 10 (D10Mit15) exhibited epistatic interactions with loci on chromosomes 9 and 16 (D9Mit10 and D16Mit182). In a second example, a locus on chromosome 12 (D12Mit167) depended on the specific combination of alleles inherited from both male and female parents. Our results show that the common laboratory mouse strains are polymorphic at loci that produce substantial differences in life span and that these effects can be sex specific and conditional on alleles inherited at other loci.
منابع مشابه
Marker loci associated with life span in genetically heterogeneous mice.
BACKGROUND Little is known about the number or chromosomal location of genetic loci that might identify individuals destined to have a long life span. Analysis of gene/life span associations in mice, which are short-lived compared to humans, might provide guidance for an analysis of the genetic basis of life span in humans. METHODS A group of 144 genetically heterogeneous mice, produced by a ...
متن کاملMapping quantitative trait loci affecting life history traits in the nematode Caenorhabditis elegans.
We have identified chromosomal regions containing quantitative trait loci (QTLs) specifying life history traits in recombinant-inbred strains of the nematode Caenorhabditis elegans. This approach also allows us to examine epistatic interactions between loci and pleiotropic effects on different traits at specific loci. QTLs for mean life span were identified on chromosomes II (near stP101), IV (...
متن کاملQuantitative trait loci for life span in Drosophila melanogaster: interactions with genetic background and larval density.
The genetic architecture of variation in adult life span was examined for a population of recombinant inbred lines, each of which had been crossed to both inbred parental strains from which the lines were derived, after emergence from both high and low larval density. QTL affecting life span were mapped within each sex and larval density treatment by linkage to highly polymorphic roo-transposab...
متن کاملAnalysis of the epistatic and QTL×environments interaction effects of plant height in maize (Zea mays L.)
A genetic map containing 103 microsatellite loci and 200 F2 plants derived from the cross R15 × Ye478 were used for mapping of quantitative trait loci (QTL) in maize (Zea mays L.). QTLs were characterized in a population of 200 F2:4 lines, derived from selfing the F2 plants, and were evaluated with two replications in two environments. QTL mapping analysis of plant height was performed by using...
متن کاملQuantitative and Molecular Genetic Analyses of Mutations Increasing Drosophila Life Span
Understanding the genetic and environmental factors that affect variation in life span and senescence is of major interest for human health and evolutionary biology. Multiple mechanisms affect longevity, many of which are conserved across species, but the genetic networks underlying each mechanism and cross-talk between networks are unknown. We report the results of a screen for mutations affec...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- The journals of gerontology. Series A, Biological sciences and medical sciences
دوره 57 1 شماره
صفحات -
تاریخ انتشار 2002