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一个调控位点Hdc - e决定了小鼠肾脏组氨酸脱羧酶对雌激素的反应。

A regulatory locus, Hdc-e, determines the response of mouse kidney histidine decarboxylase to estrogen.

作者信息

Martin S A, Bulfield G

出版信息

Biochem Genet. 1984 Dec;22(11-12):1037-46. doi: 10.1007/BF00499630.

Abstract

Levels of histidine decarboxylase (HDC; EC 4.1.1.22) activity in female mouse kidney are modulated by estrogen (administered as implanted pellets). In some inbred strains HDC activity is induced by estrogen, while in others the enzyme is repressed. Immunoprecipitation with an anti-fetal rat HDC antiserum has shown that induction and repression of HDC levels are due to changes in enzyme concentration. Segregation analysis has identified a single additively inherited regulatory locus, Hdc-e, which determines the response to estrogen. The allele Hdc-eb (C57BL/10) determines induction, and the allele Hdc-ed (DBA/2) determines repression. Preliminary evidence indicates cosegregation of Hdc-e alleles with alleles of another regulatory locus, Hdc-c (determining kidney HDC concentration), and therefore putative linkage of Hdc-e with the HDC gene complex on chromosome 2. This is the first report of a mammalian regulatory gene controlling two opposite mechanisms, induction and repression in response to a single effector.

摘要

雌性小鼠肾脏中的组氨酸脱羧酶(HDC;EC 4.1.1.22)活性受雌激素(以植入微丸形式给予)调节。在一些近交系中,HDC活性由雌激素诱导,而在其他近交系中该酶受到抑制。用抗胎鼠HDC抗血清进行免疫沉淀表明,HDC水平的诱导和抑制是由于酶浓度的变化。分离分析确定了一个单一的加性遗传调控位点Hdc - e,它决定了对雌激素的反应。等位基因Hdc - eb(C57BL/10)决定诱导作用,等位基因Hdc - ed(DBA/2)决定抑制作用。初步证据表明Hdc - e等位基因与另一个调控位点Hdc - c(决定肾脏HDC浓度)的等位基因共分离,因此推测Hdc - e与2号染色体上的HDC基因复合体存在连锁关系。这是关于一个哺乳动物调控基因控制两种相反机制(即对单一效应物的诱导和抑制)的首次报道。

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