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携带亮耳和淡耳突变等位基因双纯合的小鼠的色素沉着和溶酶体表型。

Pigmentation and lysosomal phenotypes in mice doubly homozygous for both light-ear and pale-ear mutant alleles.

作者信息

Meisler M H, Wanner L, Strahler J

出版信息

J Hered. 1984 Mar-Apr;75(2):103-6. doi: 10.1093/oxfordjournals.jhered.a109881.

Abstract

We have developed a new strain of mice homozygous for mutant alleles at both the light-ear locus on chromosome 5 and the pale-ear locus on chromosome 19. The pigmentation pattern of the double mutants, designated light-pale, is indistinguishable from the parental type. Elevated concentrations of lysosomal enzymes observed in certain tissues of the light-ear and pale-ear singly homozygous mice also are present in the double mutants, and are quantitatively indistinguishable from either parent. Although both mutations have pleiotropic effects on organelles in several tissues, neither locus influences the secretion of pancreatic zymogen granules. The close similarity in phenotypes of light ear, pale ear, and light-pale mice suggest that the le and ep loci encode different subunits of a multimeric protein, and that mutations affecting either subunit result in comparable losses of function.

摘要

我们培育出了一种新的小鼠品系,它在5号染色体上的亮耳位点和19号染色体上的淡耳位点均为突变等位基因的纯合子。这种双突变体(命名为亮-淡)的色素沉着模式与亲本类型没有区别。在亮耳和淡耳单基因纯合小鼠的某些组织中观察到的溶酶体酶浓度升高,在双突变体中也存在,并且在数量上与任一亲本没有区别。尽管这两种突变对多个组织中的细胞器都有多效性影响,但两个位点都不影响胰腺酶原颗粒的分泌。亮耳、淡耳和亮-淡小鼠在表型上的密切相似性表明,le和ep位点编码一种多聚体蛋白的不同亚基,并且影响任一亚基的突变都会导致功能的类似丧失。

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