Du X Z, Zhou L, Zhao H B, Wang Y F, Gui J F
College of Life Sciences, Central China Normal University, Wuhan 430079, China.
Fish Physiol Biochem. 2008 Jun;34(2):175-84. doi: 10.1007/s10695-007-9158-1. Epub 2007 Aug 1.
Hir/Hira (histone regulation) genes were first identified in yeast as negative regulators of histone gene expression. It has been confirmed that HIRA is a conserved family of proteins present in various animals and plants. In this paper, the cDNAs of the Hira homolog named CagHira and CaHira were isolated from gynogenetic gibel carp (gyno-carp) and gonochoristic color crucian carp (gono-carp) respectively. The full-length CagHira is 3,860 bp in length with an open reading frame (ORF) of 3,033 bp that encodes 1,011 amino acids, while the full-length CaHira is 3,748 bp in length and also has an ORF of 3,033 bp. The deduced amino acid sequences of both Hira homologs contain seven WD domains and show high identity with other HIRA family members. RT-PCR analyses revealed strong expression of Hira in the ovaries, whereas no expression was detected in the testes of either of the fishes. Hira transcription was not detected in the liver of gyno-carp, but a high level of Hira mRNA was observed in gono-carp. The temporal expression pattern showed that the Hira mRNA is consistently expressed during all embryonic development stages in gyno-carp. However, the abundance of CaHira mRNA significantly decreased (P < 0.05) shortly after fertilization and then increased again and remained stable from gastrula till hatching. The varying spatiotemporal expression patterns of Hira genes in gyno-carp and gono-carp may be associated with the differing reproductive modes used by these two closely related fishes. Our results suggest that Hira may play a role not only in the decondensation of sperm nucleus and the formation of pronucleus during fertilization, but also in gastrulation and the subsequent development of embryos.
Hir/Hira(组蛋白调控)基因最初在酵母中被鉴定为组蛋白基因表达的负调控因子。现已证实,HIRA是存在于各种动植物中的一个保守蛋白家族。在本文中,分别从雌核发育银鲫(雌核鱼)和雌雄异体彩鲫(雌雄异体鱼)中分离出了名为CagHira和CaHira的Hira同源基因的cDNA。全长CagHira为3860 bp,开放阅读框(ORF)为3033 bp,编码1011个氨基酸,而全长CaHira为3748 bp,同样具有3033 bp的ORF。两种Hira同源基因推导的氨基酸序列均包含7个WD结构域,并且与其他HIRA家族成员具有高度同源性。RT-PCR分析显示,Hira在两种鱼的卵巢中均有强烈表达,而在睾丸中未检测到表达。在雌核鱼的肝脏中未检测到Hira转录,但在雌雄异体鱼中观察到高水平的Hira mRNA。时间表达模式表明,Hira mRNA在雌核鱼的所有胚胎发育阶段均持续表达。然而,CaHira mRNA的丰度在受精后不久显著下降(P < 0.05),然后再次上升,并从原肠胚期直至孵化期保持稳定。Hira基因在雌核鱼和雌雄异体鱼中不同的时空表达模式可能与这两种亲缘关系密切的鱼类所采用的不同繁殖方式有关。我们的结果表明,Hira可能不仅在受精过程中精子核的解聚和原核的形成中发挥作用,而且在原肠胚形成及随后的胚胎发育中也发挥作用。