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血管紧张素转换酶缺陷小鼠生育能力和血压的性别差异。

Male-female differences in fertility and blood pressure in ACE-deficient mice.

作者信息

Krege J H, John S W, Langenbach L L, Hodgin J B, Hagaman J R, Bachman E S, Jennette J C, O'Brien D A, Smithies O

机构信息

Department of Internal Medicine, University of North Carolina at Chapel Hill 27599-7525, USA.

出版信息

Nature. 1995 May 11;375(6527):146-8. doi: 10.1038/375146a0.

Abstract

Angiotensin-converting enzyme (ACE) is a dipeptidyl carboxy-peptidase that generates the vasoconstricting peptide angiotensin II and inactivates the vasodilating peptide bradykinin. The gene encoding ACE is composed of two homologous regions and codes for both a somatic and testis isoenzyme. Experiments with hypertensive rats and some, but not other, studies of humans suggest that sequences at or linked to the gene influence blood pressure. The testis-specific form of ACE has its own promoter within intron 12 (ref. 14), is encoded by the 3' region of the gene, and is found only in postmeiotic spermatogenic cells and sperm. Its function is unknown. Here we investigate the role of the Ace gene in blood pressure control and reproduction using mice generated to carry an insertional mutation that is designed to inactivate both forms of ACE. All homozygous female mutants were found to be fertile, but the fertility of homozygous male mutants was greatly reduced. Heterozygous males but not females had blood pressures that were 15-20 mm Hg less than normal, although both male and female heterozygotes had reduced serum ACE activity.

摘要

血管紧张素转换酶(ACE)是一种二肽基羧肽酶,它能生成血管收缩肽血管紧张素II,并使血管舒张肽缓激肽失活。编码ACE的基因由两个同源区域组成,编码一种体细胞型和一种睾丸型同工酶。对高血压大鼠的实验以及对人类的一些(但不是其他所有)研究表明,该基因处或与之连锁的序列会影响血压。睾丸特异性形式的ACE在第12内含子中有其自身的启动子(参考文献14),由该基因的3'区域编码,并且仅在减数分裂后的生精细胞和精子中发现。其功能尚不清楚。在这里,我们使用通过携带旨在使两种形式的ACE均失活的插入突变而产生的小鼠,研究Ace基因在血压控制和生殖中的作用。发现所有纯合雌性突变体都具有生育能力,但纯合雄性突变体的生育能力大大降低。杂合雄性而非雌性的血压比正常血压低15 - 20毫米汞柱,尽管雄性和雌性杂合子的血清ACE活性均降低。

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