López-Alãnón D M, Lopez-Fernández L A, Castañeda V, Krimer D B, Del Mazo J
Department of Cell and Developmental Biology, Centro de Investigaciones Biológicas (C.S.I.C.), Madrid, Spain.
DNA Cell Biol. 1997 May;16(5):639-44. doi: 10.1089/dna.1997.16.639.
Replacement-variant H3.3 histones have been isolated and sequenced in different eukaryotes, but no functional H3.3A gene has been characterized in the mouse so far. We have cloned an H3.3A cDNA from a mouse fetal ovary library, differentially screened with testis versus somatic cDNA probes. We showed this gene contains a region homologous to the reverse and complementary alpha-globin gene. We believe such a structure could have been generated by retroposition during the evolution of both globin and histone gene families. The sequence coding for H3.3A is 76.6% homologous to the mouse H3.3B gene at the nucleotide level and differs in only one amino acid at the protein level. The high degree of homology between these genes and the H3.3 variant histones from other eukaryotes reveals the conservation of these replication-independent class of histones throughout evolution. Analysis of gene expression reveals a developmental regulation concurrent with meiotic progression, with the highest level of transcript detection coincident with meiotic onset during both oogenesis and spermatogenesis.
在不同的真核生物中已经分离并测序了替代变体H3.3组蛋白,但到目前为止,小鼠中尚未鉴定出功能性的H3.3A基因。我们从一个小鼠胎儿卵巢文库中克隆了一个H3.3A cDNA,用睾丸与体细胞cDNA探针进行差异筛选。我们发现该基因包含一个与反向互补α-珠蛋白基因同源的区域。我们认为这种结构可能是在珠蛋白和组蛋白基因家族的进化过程中通过逆转座产生的。编码H3.3A的序列在核苷酸水平上与小鼠H3.3B基因有76.6%的同源性,在蛋白质水平上仅相差一个氨基酸。这些基因与其他真核生物的H3.3变体组蛋白之间的高度同源性揭示了这些不依赖复制的组蛋白在整个进化过程中的保守性。基因表达分析显示,其与减数分裂进程同步进行发育调控,在卵子发生和精子发生过程中,转录本检测的最高水平与减数分裂开始一致。