Sittman D B, Chiu I M, Pan C J, Cohn R H, Kedes L H, Marzluff W F
Proc Natl Acad Sci U S A. 1981 Jul;78(7):4078-82. doi: 10.1073/pnas.78.7.4078.
Histone mRNA was partially purified from mouse myeloma cells synchronized in S phase by isoleucine starvation. A cDNA was prepared that contained sequences complementary to all five mouse histone genes. This cDNA was used to screen a library of mouse DNA in lambda phage. The positive clones were screened by hybridization with sea urchin histone gene-specific probes to identify those clones that contained histone genes. Confirmation of this identification was obtained by hybridization with Drosophila histone genes. Two independent clusters of histone genes were isolated. One, MM531, contains regions hybridizing specifically to H3, H4, and H1 and the other, MM221, contains two regions hybridizing specifically to H3 and single regions complementary to H4, H2b, and H2a. They are not part of a simple repeating structure. The nucleotide sequence of the coding region of the H3 gene in MM531 has been determined. This gene could code for a variant H3 protein that has several amino acid substitutions not reported in other H3 proteins.
组蛋白mRNA是从经异亮氨酸饥饿同步于S期的小鼠骨髓瘤细胞中部分纯化得到的。制备了一个cDNA,其包含与所有五个小鼠组蛋白基因互补的序列。该cDNA用于筛选λ噬菌体中的小鼠DNA文库。通过与海胆组蛋白基因特异性探针杂交来筛选阳性克隆,以鉴定那些含有组蛋白基因的克隆。通过与果蝇组蛋白基因杂交获得了该鉴定的确认。分离出了两个独立的组蛋白基因簇。一个是MM531,包含与H3、H4和H1特异性杂交的区域;另一个是MM221,包含两个与H3特异性杂交的区域以及与H4、H2b和H2a互补的单个区域。它们不是简单重复结构的一部分。已经确定了MM531中H3基因编码区的核苷酸序列。该基因可以编码一种变体H3蛋白,该蛋白具有一些在其他H3蛋白中未报道的氨基酸取代。