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小鼠T/t复合体内的基因定位。I. t致死基因是非等位基因。

Gene mapping within the T/t complex of the mouse. I. t-Lethal genes are nonallelic.

作者信息

Artzt K, McCormick P, Bennett D

出版信息

Cell. 1982 Mar;28(3):463-70. doi: 10.1016/0092-8674(82)90200-8.

Abstract

The t haplotypes of mouse chromosome 17 are natural polymorphisms in wild populations that contain mutations that affect or control such diverse functions as tail length, embryonic lethality and maturation and function of male germ cells. The major impediment to dissecting the genetics of this complex region has been its unusual property of recombination suppression in heterozygotes with wild-type chromosomes. Recently it was shown that recombination suppression does not occur in heterozygotes containing two different t haplotypes, which suggested that t chromosomes may be mismatched with respect to wild-type but share sequences that permit crossing-over between them. Thus for the first time questions of allelism and map positions of the t-lethal mutations can be addressed. We report here the results of three experiments that analyzed the tw12 haplotype trans to either tw5, tw32 or tw18. In all cases these lethal mutations were nonallelic to tw12. These results, together with evidence for functional relatedness, suggest the t-lethals may be a gene family spread out over more than 15 centiMorgans of chromosome 17.

摘要

小鼠17号染色体的t单倍型是野生种群中的自然多态性,其中包含影响或控制诸如尾巴长度、胚胎致死率以及雄性生殖细胞成熟和功能等多种不同功能的突变。剖析这个复杂区域遗传学的主要障碍一直是其在与野生型染色体的杂合子中具有异常的重组抑制特性。最近有研究表明,在含有两种不同t单倍型的杂合子中不会发生重组抑制,这表明t染色体与野生型可能在序列上不匹配,但它们共享允许它们之间发生交叉互换的序列。因此,首次可以解决t致死突变的等位性和图谱位置问题。我们在此报告了三个实验的结果,这些实验分析了与tw5、tw32或tw18反式的tw12单倍型。在所有情况下,这些致死突变与tw12是非等位的。这些结果,连同功能相关性的证据,表明t致死基因可能是一个分布在17号染色体超过15厘摩区域的基因家族。

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