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通过测序分析克隆的海胆组蛋白DNA的基因和间隔区。

Genes and spacers of cloned sea urchin histone DNA analyzed by sequencing.

作者信息

Schaffner W, Kunz G, Daetwyler H, Telford J, Smith H O, Birnstiel M L

出版信息

Cell. 1978 Jul;14(3):655-71. doi: 10.1016/0092-8674(78)90249-0.

Abstract

A cloned histone gene cluster of the highly reiterated type from the sea urchin Psammechinus miliaris was analyzed by DNA sequencing. More than half of the 6 kb repeat was sequenced, including coding regions of all five histones, some prelude and trailing sequences lying adjacent to the structural gense, and segments of the AT-rich spacer DNA. The gene cluster does not code for gonad-specific histone variants but may instead be active in early sea urchin development, as indicated by comparison to reference histones. The encoded histones seem not to be derived from longer precursor proteins, not is there any evidence for insert sequences within the coding regions. Sequence similarities exist among the putative ribosome-binding sites adjacent to the initiator codons of individual genes. The AT-rich spacer segments between the genes differ from each other, are made up from relatively simple nucleotide arrangements, but are not repetitious, and apparently do not code for additional large proteins.

摘要

对来自海胆米氏刻肋海胆的高度重复型克隆组蛋白基因簇进行了DNA测序分析。对6 kb重复序列的一半以上进行了测序,包括所有五种组蛋白的编码区、位于结构基因相邻位置的一些前导和尾随序列,以及富含AT的间隔DNA片段。该基因簇不编码性腺特异性组蛋白变体,而是可能在海胆早期发育中活跃,与参考组蛋白的比较表明了这一点。编码的组蛋白似乎不是来自更长的前体蛋白,编码区内也没有插入序列的证据。各个基因起始密码子相邻的假定核糖体结合位点之间存在序列相似性。基因之间富含AT的间隔片段彼此不同,由相对简单的核苷酸排列组成,但不重复,显然也不编码额外的大蛋白。

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