Schulze E, Nagel S, Gavenis K, Grossbach U
Third Department of Zoology Developmental Biology, University of Göttingen, Germany.
J Cell Biol. 1994 Dec;127(6 Pt 2):1789-98. doi: 10.1083/jcb.127.6.1789.
Condensed and late-replicating interphase chromatin in the Dipertan insect Chironomus contains a divergent type of histone H1 with an inserted KAP-KAP repeat that is conserved in single H1 variants of Caenorhabditis elegans and Volvox carteri. H1 peptides comprising the insertion interact specifically with DNA. The Chironomid Glyptotendipes exhibits a corresponding correlation between the presence of condensed chromosome sections and the appearance of a divergent H1 subtype. The centromere regions and other sections of Glyptotendipes barbipes chromosomes are inaccessible to immunodecoration by anti-H2B and anti-H1 antibodies one of which is known to recognize nine different epitopes in all domains of the H1 molecule. Microelectrophoresis of the histones from manually isolated unfixed centromeres revealed the presence of H1 and core histones. H1 genes of G. barpipes were sequenced and found to belong to two groups. H1 II and H1 III are rather similar but differ remarkably from H1 I. About 30% of the deduced amino acid residues were found to be unique to H1 I. Most conspicuous is the insertion, SPAKSPGR, in H1 I that is lacking in H1 II and H1 III and at its position gives rise to the sequence repeat SPAKSPAKSPGR. The homologous H1 I gene in Glyptotendipes salinus encodes the very similar repeat TPAKSPAKSPGR. Both sequences are structurally related to the KAPKAP repeat in H1 I-1 specific for condensed chromosome sites in Chironomus and to the SPKKSPKK repeat in sea urchin sperm H1, lie at almost the same distance from the central globular domain, and could interact with linker DNA in packaging condensed chromatin.
双翅目昆虫摇蚊的浓缩且复制后期的间期染色质含有一种不同类型的组蛋白H1,其插入了KAP-KAP重复序列,该序列在秀丽隐杆线虫和团藻的单个H1变体中保守。包含插入序列的H1肽与DNA特异性相互作用。摇蚊属的雕翅摇蚊在浓缩染色体节段的存在与不同的H1亚型的出现之间表现出相应的相关性。巴氏摇蚊染色体的着丝粒区域和其他节段不能被抗H2B和抗H1抗体免疫标记,其中一种抗体已知可识别H1分子所有结构域中的九个不同表位。对人工分离的未固定着丝粒的组蛋白进行微电泳,结果显示存在H1和核心组蛋白。对巴氏摇蚊的H1基因进行测序,发现其属于两组。H1 II和H1 III相当相似,但与H1 I明显不同。发现推导的氨基酸残基中约30%是H1 I所特有的。最明显的是H1 I中的插入序列SPAKSPGR,H1 II和H1 III中没有该序列,在其位置产生序列重复SPAKSPAKSPGR。盐沼摇蚊中的同源H1 I基因编码非常相似的重复序列TPAKSPAKSPGR。这两个序列在结构上与摇蚊中对浓缩染色体位点特异的H1 I-1中的KAPKAP重复序列以及海胆精子H1中的SPKKSPKK重复序列相关,与中央球状结构域的距离几乎相同,并且可能在包装浓缩染色质时与连接DNA相互作用。