首页> 美国卫生研究院文献>Nucleic Acids Research >Molecular cloning and carboxyl-propeptide analysis of human type III procollagen.
【2h】

Molecular cloning and carboxyl-propeptide analysis of human type III procollagen.

机译:人类III型前胶原的分子克隆和羧基前肽分析。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Two human cDNA libraries prepared from normal fibroblast (GM3348) and rhabdomyosarcoma (CCL136) mRNAs were screened under cross hybridization conditions with a genomic fragment coding for exons 2 and 3 of the avian type III procollagen COOH-propeptide (Yamada, Y., Mudryj, M., Sullivan, M. and deCrombrugghe, B. (1983) J. Biol. Chem. 258, 2758-2761). One cDNA clone containing a 1.12 kb insert was isolated from the CCL136 library and later used to identify a GM3348 derived clone with a 2.4 kb insert. Comparison of the human and avian type III C-terminal propeptides revealed much more divergence in the first 54 amino acids following the terminal cysteine of the triple helical region than is present in the alpha 1(I) and alpha 2(I) procollagen chains of these species. Analysis of poly (A+) RNA from normal human fibroblast and tumor cell lines showed that they differed greatly in the relative amounts of alpha 1(I), alpha 2(I), and alpha 1(III) mRNAs. Furthermore, as we previously reported for the alpha 1(I) and alpha 2(I) transcripts, multiple mRNAs also hybridize to the cloned alpha 1(III) DNA.
机译:在交叉杂交条件下,用编码禽类III型原胶原COOH-前肽外显子2和3的基因组片段筛选了由正常成纤维细胞(GM3348)和横纹肌肉瘤(CCL136)mRNA制备的两个人cDNA文库(Yamada,Y.,Mudryj, M.,Sullivan,M。和deCrombrugghe,B。(1983)J.Biol.Chem.258,2758-2761)。从CCL136文库中分离出一个包含1.12 kb插入片段的cDNA克隆,随后用于鉴定具有2.4 kb插入片段的GM3348衍生克隆。人类和禽类III C末端前肽的比较显示,在三螺旋区末端半胱氨酸之后的前54个氨基酸中,前者的α1(I)和α2(I)前胶原链中存在更多的分歧。这些物种。对来自正常人成纤维细胞和肿瘤细胞系的多聚(A +)RNA的分析表明,它们在alpha 1(I),alpha 2(I)和alpha 1(III)mRNA的相对量上存在很大差异。此外,正如我们先前报道的alpha 1(I)和alpha 2(I)转录本一样,多个mRNA也与克隆的alpha 1(III)DNA杂交。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号