van Daal A, White E M, Gorovsky M A, Elgin S C
Department of Biology, Washington University, St Louis, MO 63130.
Nucleic Acids Res. 1988 Aug 11;16(15):7487-97. doi: 10.1093/nar/16.15.7487.
The Tetrahymena histone H2A variant designated hv1 is localized exclusively in the transcriptionally active macronucleus and is absent from the quiescent micronucleus (1). A cDNA clone of the hv1 gene (2) was used to screen a Drosophila cDNA library. A cross-hybridizing clone was recovered and shown by sequence analysis to code for a protein homologous to hv1 as well as to the chicken H2A variant, H2A.F (3), the sea urchin H2A variant, H2A.F/Z (4) and the mammalian H2A variant H2A.Z (5). Southern analysis of Drosophila genomic DNA indicates that the H2AvD (H2A variant Drosophila) gene is present in one copy. In situ hybridization places the locus at 97CD on chromosome 3, while the S-phase regulated histone genes are on chromosome 2 (6). Thus the Drosophila H2A variant should be accessible to genetic analysis, which will enable its function to be determined.
被命名为hv1的嗜热四膜虫组蛋白H2A变体仅定位于转录活跃的大核中,而静止的小核中则不存在(1)。hv1基因的一个cDNA克隆(2)被用于筛选果蝇cDNA文库。回收了一个交叉杂交克隆,通过序列分析表明它编码一种与hv1以及鸡H2A变体H2A.F(3)、海胆H2A变体H2A.F/Z(4)和哺乳动物H2A变体H2A.Z(5)同源的蛋白质。对果蝇基因组DNA的Southern分析表明,H2AvD(果蝇H2A变体)基因以单拷贝形式存在。原位杂交将该基因座定位于3号染色体的97CD处,而S期调控的组蛋白基因位于2号染色体上(6)。因此,果蝇H2A变体应该可以进行遗传分析,这将有助于确定其功能。