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大鼠嗜铬细胞瘤PC12细胞组蛋白H1(0)编码基因编码区的克隆与分析

Cloning and analysis of the coding region of the histone H1(0)-encoding gene from rat PC12 cells.

作者信息

Martínez P, Vidal J M, Monsalves C, Pérez M, Pucket C, Ponte I, Suau P

机构信息

Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad Autonóma de Barcelona, Bellaterra, Spain.

出版信息

Gene. 1995 Dec 12;166(2):313-6. doi: 10.1016/0378-1119(95)00594-3.

Abstract

We have determined the complete coding sequence of the histone-encoding H1(0) gene from rat PC12 cells. Southern and Northern analyses suggest that rat H1(0) is encoded by a single-copy gene which generates an mRNA of about 2.2 kb. Comparison of the rat, mouse and human amino-acid sequences shows that the C-terminal domain of the protein is much more variable than the N-terminal and central domains. Rates of non-synonymous and synonymous nucleotide substitution have been calculated. The rate of non-synonymous substitution is about 2.5-times higher in the rodent lineage than in the human lineage.

摘要

我们已经确定了大鼠PC12细胞中组蛋白编码H1(0)基因的完整编码序列。Southern和Northern分析表明,大鼠H1(0)由一个单拷贝基因编码,该基因产生约2.2 kb的mRNA。大鼠、小鼠和人类氨基酸序列的比较表明,该蛋白质的C末端结构域比N末端和中央结构域的变异性大得多。已经计算了非同义核苷酸替换和同义核苷酸替换的速率。啮齿动物谱系中的非同义替换率比人类谱系中的高约2.5倍。

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