首页> 美国卫生研究院文献>Nucleic Acids Research >Cloning and analysis of cDNA sequences coding for two 16 kilodalton heat shock proteins (hsps) in Caenorhabditis elegans: homology with the small hsps of Drosophila.
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Cloning and analysis of cDNA sequences coding for two 16 kilodalton heat shock proteins (hsps) in Caenorhabditis elegans: homology with the small hsps of Drosophila.

机译:秀丽隐杆线虫中编码两个16千道尔顿热激蛋白(hsps)的cDNA序列的克隆和分析:与果蝇的小hps同源。

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摘要

The nucleotide sequences of two different cDNAs, CEHS48 and CEHS41, coding for the 16,000 dalton heat shock proteins (hsps) of Caenorhabditis elegans have been determined. CEHS48 codes for a polypeptide of 135 amino acids, approximately 15 fewer than the complete protein while CEHS41 is missing approximately 46 amino acids. From nucleotide 113 to the TAA termination signal the extent of homology between the sequences is 91%. Toward the 5' ends, the homology drops to 20% and results in completely divergent amino acid sequences. The 3' noncoding regions are only 30% homologous. Only CEHS48 contains a poly(A) signal and a poly(A) tail, suggesting that CEHS41 has an incomplete 3' end. The region from amino acid 43 to amino acid 115 shows extensive homology with corresponding regions in the four small hsps of Drosophila melanogaster and in mammalian alpha-crystallin. Two-dimensional gel analysis of in vitro synthesized hsp16 reveals the existence of five distinct components of identical molecular weights, but with different isoelectric points.
机译:已确定编码秀丽隐杆线虫的16,000道尔顿热休克蛋白(hsps)的两种不同cDNA CEHS48和CEHS41的核苷酸序列。 CEHS48编码135个氨基酸的多肽,比完整蛋白质少约15个氨基酸,而CEHS41缺失约46个氨基酸。从核苷酸113到TAA终止信号,序列之间的同源性程度为91%。朝向5'端,同源性下降至20%,并导致氨基酸序列完全不同。 3'非编码区仅30%同源。只有CEHS48包含poly(A)信号和poly(A)尾巴,表明CEHS41具有不完整的3'末端。从氨基酸43到氨基酸115的区域与果蝇的四个小hsps和哺乳动物α-晶状体蛋白中的相应区域显示出广泛的同源性。体外合成的hsp16的二维凝胶分析揭示了分子量相同但等电点不同的五个不同组分的存在。

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