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同基因小鼠寿命调控的遗传因素分析。

An analysis of genetic factors regulating life-span in congeneic mice.

作者信息

Popp D M

出版信息

Mech Ageing Dev. 1982 Feb;18(2):125-34. doi: 10.1016/0047-6374(82)90082-3.

Abstract

Controlled matings between two strains of mice that have minimum genetic heterogeneity but whose mean ages at death are significantly different were used to identify genetic factors that govern longevity. The congeneic pair, C57BL/10 (B10) and C57BL/10.F (B10.F), differ at a region of the genome in and around the H-2 complex and have mean ages at death of 706 +/- 14 and 456 +/- 15 days, respectively. B10.F also has a reduced level of basal serum IgA levels, a trait which segregates in F2 progeny. F2 and back-cross progeny were classified for the H-2 genotype and allowed to live out their life-span. Survival curves for F2 and backcross progeny selected on the basis of their H-2 type show that the progeny homozygous for the H-2 allele of B10.F have a mean age at death significantly different and reduced from that of the progeny homozygous for the H-2 allele of B10.

摘要

为了确定控制寿命的遗传因素,研究人员选用了两种小鼠品系进行受控交配。这两种小鼠品系的遗传异质性最低,但平均死亡年龄却有显著差异。同源近交系C57BL/10(B10)和C57BL/10.F(B10.F)在H-2复合体及其周围的基因组区域存在差异,它们的平均死亡年龄分别为706±14天和456±15天。B10.F的基础血清IgA水平也较低,这一性状在F2后代中会发生分离。对F2和回交后代进行H-2基因型分类,并让它们自然寿命终结。根据H-2类型选择的F2和回交后代的生存曲线表明,B10.F的H-2等位基因纯合后代的平均死亡年龄与B10的H-2等位基因纯合后代相比,有显著差异且更低。

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