Sures I, Lowry J, Kedes L H
Cell. 1978 Nov;15(3):1033-44. doi: 10.1016/0092-8674(78)90287-8.
The DNA sequence of two cloned segments of the histone gene repeat unit of the sea urchin S. purpuratus has been determined. One sequence contains the contiguous H2B and H3 genes and their interdigitated spacer regions; the other comprises the H2A gene and flanking spacer sequences. Analysis of the coding regions reveals a methionine residue within the H2A protein. H2A, which generally lacks this amino acid, contains methionine only in a protein variant which is synthesized in early sea urchin embryogenesis. We thus conclude that the cloned DNA represents a set of genes which is active early in development. Codon selection is markedly skewed and similar for each of the three genes. The DNA sequences are co-linear with known histone protein sequences and-unlike several other eucaryotic genes-do not show any insertions in the coding regions. The spacer regions are relatively AT-rich although GC cluster are scattered throughout. Several short stretches of homology are found in regions both upstream and downstream from the protein coding segments. The conservation of these sequences and their location at analogous sites suggest that they are involved in gene transcription or in mRNA translation. No tandem or dispersed repeats were found, with the exception of the remarkable sequence having the structure located in the spacer between the H2A and H1 genes.
已确定了海胆紫球海胆(Strongylocentrotus purpuratus)组蛋白基因重复单元的两个克隆片段的DNA序列。一个序列包含相邻的H2B和H3基因及其相互交错的间隔区;另一个包含H2A基因和侧翼间隔序列。对编码区的分析揭示了H2A蛋白内的一个甲硫氨酸残基。通常缺乏这种氨基酸的H2A,仅在海胆胚胎发育早期合成的一种蛋白质变体中含有甲硫氨酸。因此,我们得出结论,克隆的DNA代表了一组在发育早期活跃的基因。密码子选择明显偏向,并且这三个基因中的每一个都相似。DNA序列与已知的组蛋白蛋白质序列共线性,并且与其他几个真核基因不同,在编码区没有显示任何插入。间隔区相对富含AT,尽管GC簇分散在各处。在蛋白质编码片段的上游和下游区域都发现了几段短的同源序列。这些序列的保守性及其在类似位点的位置表明它们参与基因转录或mRNA翻译。除了位于H2A和H1基因之间间隔区的具有该结构的显著序列外,未发现串联或分散重复序列。