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小鼠印度刺猬蛋白的翻译后加工及在肾脏中的表达

Post-translational processing and renal expression of mouse Indian hedgehog.

作者信息

Valentini R P, Brookhiser W T, Park J, Yang T, Briggs J, Dressler G, Holzman L B

机构信息

Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan 48109-0676, USA.

出版信息

J Biol Chem. 1997 Mar 28;272(13):8466-73. doi: 10.1074/jbc.272.13.8466.

Abstract

The full-length mouse Indian hedgehog (Ihh) cDNA was cloned from an embryonic 17.5-day kidney library and was used to study the post-translational processing of the peptide and temporal and spatial expression of the transcript. Sequence analysis predicted two putative translation initiation sites. Ihh translation was initiated at both initiation sites when expressed in an in vitro transcription/translation system. Expression of an Ihh mutant demonstrated that the internal translation initiation site was sufficient to produce the mature forms of Ihh. Ihh post-translational processing proceeded in a fashion similar to Sonic and Drosophila hedgehog; the unprocessed form underwent signal peptide cleavage as well as internal proteolytic processing to form a 19-kDa amino-terminal peptide and a 26-kDa carboxyl-terminal peptide. This processing required His313 present in a conserved serine protease motif. Ihh transcript was detected by in situ RNA hybridization as early as 10 days postcoitum (dpc) in developing gut, as early as 14.5 dpc in the cartilage primordium, and in the developing urogenital sinus. In semiquantitative reverse transcription-polymerase chain reaction experiments, Indian hedgehog transcript was first detected in the mouse metanephros at 14.5 dpc; transcript abundance increased with gestational age, becoming maximal in adulthood. In adult kidney, Ihh transcript was detected only in the proximal convoluted tubule and proximal straight tubule.

摘要

全长小鼠印度刺猬因子(Ihh)cDNA是从胚胎17.5天的肾脏文库中克隆出来的,用于研究该肽的翻译后加工以及转录本的时空表达。序列分析预测了两个假定的翻译起始位点。在体外转录/翻译系统中表达时,Ihh在两个起始位点均起始翻译。Ihh突变体的表达表明内部翻译起始位点足以产生Ihh的成熟形式。Ihh的翻译后加工过程与音猬因子和果蝇刺猬因子相似;未加工的形式经历信号肽切割以及内部蛋白水解加工,形成一个19 kDa的氨基末端肽和一个26 kDa的羧基末端肽。这种加工需要保守丝氨酸蛋白酶基序中的His313参与。早在交配后10天(dpc),在发育中的肠道中通过原位RNA杂交检测到Ihh转录本,早在14.5 dpc在软骨原基以及发育中的泌尿生殖窦中检测到。在半定量逆转录-聚合酶链反应实验中,最早在14.5 dpc于小鼠后肾中检测到印度刺猬因子转录本;转录本丰度随胎龄增加,在成年期达到最大值。在成年肾脏中,仅在近端曲管和近端直管中检测到Ihh转录本。

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