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Genetic Loci Modulating Fitness and Life Span in Caenorhabditis elegans: Categorical Trait Interval Mapping in CL2a × Bergerac-BO Recombinant-Inbred Worms

机译:秀丽隐杆线虫适应度和寿命的遗传位点调控:CL2a×Bergerac-BO重组自交系蠕虫的分类性状区间定位

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Quantitative trait loci (QTL) can implicate an unbiased sampling of genes underlying a complex, polygenic phenotype. QTL affecting longevity in Caenorhabditis elegans were mapped using a CL2a × Bergerac-BO recombinant-inbred population. Genotypes were compared at 30 transposon-specific markers for two paired sample sets totaling 171 young controls and 172 longevity-selected worms (the last-surviving 1) from a synchronously aged population. A third sample set, totaling 161 worms from an independent culture, was analyzed for confirmation of loci. At least six highly significant QTL affecting life span were detected both by single-marker (χ2) analysis and by two interval-mapping procedures—one intended for nonparametric traits and another developed specifically for mapping of categorical traits. These life-span QTL were located on chromosomes I (near the hP4 locus), III (near stP127 ), IV (near stP44 ), V (a cluster of three peaks, near stP192, stP23 , and stP6 ), and X (two distinct peaks, near stP129 and stP2 ). Epistatic effects on longevity were also analyzed by Fisher's exact test, which indicated a significant life-span interaction between markers on chromosomes V ( stP128 ) and III ( stP127 ). Several further interactions were significant in the initial unselected population; two of these, between distal loci on chromosome V, were completely eliminated in the long-lived subset. Allelic longevity effects for two QTL, on chromosomes IV and V, were confirmed in backcrossed congenic lines and were highly significant in two very different environments—growth on solid agar medium and in liquid suspension culture.
机译:数量性状位点 (QTL) 可以对复杂的多基因表型进行无偏倚的基因采样。使用CL2a×Bergerac-BO重组自交种群绘制了影响秀丽隐杆线虫寿命的QTL。在两个配对样本集的 30 个转座子特异性标记处比较基因型,共计 171 个年轻对照和 172 个长寿选择的蠕虫(最后存活的 1%),来自同步老龄化人群。分析了第三组样本,共计 161 条来自独立培养物的蠕虫,以确认位点。通过单标记 (χ2) 分析和两个区间映射程序(一个用于非参数性状,另一个专门用于分类性状映射)检测到至少 6 个影响寿命的高度显着 QTL。这些寿命 QTL 位于染色体 I(靠近 hP4 位点)、III(靠近 stP127)、IV(靠近 stP44)、V(三个峰簇,靠近 stP192、stP23 和 stP6)和 X(两个不同的峰,靠近 stP129 和 stP2)。Fisher精确检验也分析了上位对寿命的影响,该检验表明染色体V(stP128)和III(stP127)上的标记之间存在显着的寿命相互作用。在最初的未选择人群中,进一步的相互作用是显着的;其中两个位于 V 号染色体远端位点之间,在长寿命亚群中被完全消除。两个QTL对IV号和V号染色体的等位基因长寿效应在回交的同源系中得到证实,并且在两种截然不同的环境中(固体琼脂培养基和液体悬浮培养物的生长)中具有高度显著性。

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