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编码小牛II型胶原蛋白原α1链的cDNA和基因组克隆的分析。

Analysis of cDNA and genomic clones coding for the pro alpha 1 chain of calf type II collagen.

作者信息

Sangiorgi F O, Benson-Chanda V, de Wet W J, Sobel M E, Ramirez F

出版信息

Nucleic Acids Res. 1985 Apr 25;13(8):2815-26. doi: 10.1093/nar/13.8.2815.

Abstract

A bovine cDNA library constructed from fetal cartilage RNA was screened with a pro alpha 1(II) collagen specific chicken cDNA. A recombinant clone (Bc 7), with an insert of 1 kb, was identified and shown to contain sequences exhibiting 85% homology with the chicken pro alpha 1(II) collagen C-propeptide. Interspecies comparison strongly suggested that one potential glycosylation site present in the avian C-propeptide is not utilized, since this site is absent in the bovine chain. In addition, two overlapping genomic clones (Pal 3 and Pal 4) were isolated and partially characterized. These clones span 23 kb of DNA and contain approximately 17 kb of the pro alpha 1(II) calf gene. Sequencing of exon 1 has determined the length of the 3' untranslated region and the exact location of the polyadenylation attachment site.

摘要

用鸡的原α1(II)型胶原特异性cDNA筛选由胎儿软骨RNA构建的牛cDNA文库。鉴定出一个插入片段为1 kb的重组克隆(Bc 7),并显示其包含与鸡原α1(II)型胶原C-前肽具有85%同源性的序列。种间比较强烈表明,禽类C-前肽中存在的一个潜在糖基化位点未被利用,因为该位点在牛链中不存在。此外,分离出两个重叠的基因组克隆(Pal 3和Pal 4)并进行了部分特征分析。这些克隆跨越23 kb的DNA,包含约17 kb的小牛原α1(II)型基因。外显子1的测序确定了3'非翻译区的长度和聚腺苷酸化附着位点的确切位置。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af08/341196/e09eed942186/nar00302-0147-a.jpg

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