Whitbread L A, Gregg K, Rogers G E
Department of Biochemistry, University of Adelaide, South Australia.
Gene. 1991 May 30;101(2):223-9. doi: 10.1016/0378-1119(91)90415-8.
A cDNA library was constructed from embryonic chick claw mRNA and a claw keratin (cKer)-encoding clone was isolated and sequenced. Subsequently, a genomic clone, containing four cKer-encoding genes (cKer) was isolated and one of the genes (cKer1) was completely sequenced. The cKerl gene appears to be differentially expressed in the keratinizing tissue appendages of the embryonic chick, being abundantly expressed in the claw and at a low level in feather tissue. Comparison of the deduced amino acid (aa) sequence of the cKer to those of feather (fKer) and scale keratins (sKer) showed that the regions conserved between fKer and sKer are also found in the cKer. The glycine-rich as repeat region characteristic of sKer is also present in a shortened form in the cKer sequence. Like the fKer genes (fKer) and the feather histidine-rich protein-encoding gene (HRP), the cKer1 gene also contains one intron which interrupts the 5'-noncoding region at an equivalent position to that found in the fKer and HRP genes. Genomic Southern analysis using the cKer cDNA as a probe indicated the presence of several related genes in the chick genome.
从胚胎期鸡爪的mRNA构建了一个cDNA文库,并分离和测序了一个编码爪角蛋白(cKer)的克隆。随后,分离出一个包含四个编码cKer基因(cKer)的基因组克隆,并对其中一个基因(cKer1)进行了全序列测定。cKerl基因似乎在胚胎期鸡的角质化组织附属器中差异表达,在爪中大量表达,而在羽毛组织中表达水平较低。将cKer推导的氨基酸(aa)序列与羽毛角蛋白(fKer)和鳞片角蛋白(sKer)的序列进行比较,结果表明,fKer和sKer之间保守的区域在cKer中也存在。sKer特有的富含甘氨酸的重复区域在cKer序列中也以缩短的形式存在。与fKer基因(fKer)和编码羽毛富含组氨酸蛋白的基因(HRP)一样,cKer1基因也含有一个内含子,该内含子在与fKer和HRP基因相同的位置打断5'-非编码区。用cKer cDNA作为探针进行的基因组Southern分析表明,鸡基因组中存在几个相关基因。