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果蝇Nod类染色体驱动蛋白的HhH2/NDD结构域是其在卵母细胞核中与染色体结合所必需的。

The HhH2/NDD domain of the Drosophila Nod chromokinesin-like protein is required for binding to chromosomes in the oocyte nucleus.

作者信息

Cui Wei, Hawley R Scott

机构信息

Stowers Institute for Medical Research, 1000 E. 50th Street, Kansas City, MO 64110, USA.

出版信息

Genetics. 2005 Dec;171(4):1823-35. doi: 10.1534/genetics.105.047464. Epub 2005 Sep 2.

Abstract

Nod is a chromokinesin-like protein that plays a critical role in segregating achiasmate chromosomes during female meiosis. The C-terminal half of the Nod protein contains two putative DNA-binding domains. The first of these domains, known as the HMGN domain, consists of three tandemly repeated high-mobility group N motifs. This domain was previously shown to be both necessary and sufficient for binding of the C-terminal half of Nod to mitotic chromosomes in embryos. The second putative DNA-binding domain, denoted HhH(2)/NDD, is a helix-hairpin-helix(2)/Nod-like DNA-binding domain. Although the HhH(2)/NDD domain is not required or sufficient for chromosome binding in embryos, several well-characterized nod mutations have been mapped in this domain. To characterize the role of the HhH(2)/NDD domain in mediating Nod function, we created a series of UAS-driven transgene constructs capable of expressing either a wild-type Nod-GFP fusion protein or proteins in which the HhH(2)/NDD domain had been altered by site-directed mutagenesis. Although wild-type Nod-GFP localizes to the oocyte chromosomes and rescues the segregation defect in nod mutant oocytes, two of three proteins carrying mutants in the HhH(2)/NDD domain fail to either rescue the nod mutant phenotype or bind to oocyte chromosomes. However, these mutant proteins do bind to the polytene chromosomes in nurse-cell nuclei and enter the oocyte nucleus. Thus, even though the HhH(2)/NDD domain is not essential for chromosome binding in other cell types, it is required for chromosome binding in the oocyte. These HhH(2)/NDD mutants also block the localization of Nod to the posterior pole of stage 9-10A oocytes, a process that is thought to facilitate the interaction of Nod with the plus ends of microtubules (Cui et al. 2005). This observation suggests that the Nod HhH2/NDD domain may play other roles in addition to binding Nod to meiotic chromosomes.

摘要

Nod是一种类染色体驱动蛋白,在雌性减数分裂过程中分离无交叉染色体时发挥关键作用。Nod蛋白的C端部分包含两个假定的DNA结合结构域。其中第一个结构域,即HMGN结构域,由三个串联重复的高迁移率族N基序组成。先前已证明该结构域对于Nod的C端部分与胚胎有丝分裂染色体的结合既必要又充分。第二个假定的DNA结合结构域,称为HhH(2)/NDD,是一种螺旋-发夹-螺旋(2)/Nod样DNA结合结构域。尽管HhH(2)/NDD结构域对于胚胎中的染色体结合并非必需或充分,但已在该结构域中定位了几个特征明确的nod突变。为了表征HhH(2)/NDD结构域在介导Nod功能中的作用,我们创建了一系列UAS驱动的转基因构建体,能够表达野生型Nod-GFP融合蛋白或其中HhH(2)/NDD结构域已通过定点诱变改变的蛋白。虽然野生型Nod-GFP定位于卵母细胞染色体并挽救nod突变卵母细胞中的分离缺陷,但携带HhH(2)/NDD结构域突变的三种蛋白中的两种既未能挽救nod突变表型,也未能与卵母细胞染色体结合。然而,这些突变蛋白确实与滋养细胞核中的多线染色体结合并进入卵母细胞核。因此,即使HhH(2)/NDD结构域对于其他细胞类型中的染色体结合并非必不可少,但它对于卵母细胞中的染色体结合却是必需的。这些HhH(2)/NDD突变体还阻止了Nod定位于9-10A期卵母细胞的后极,这一过程被认为有助于Nod与微管正端的相互作用(Cui等人,2005年)。这一观察结果表明,Nod HhH2/NDD结构域除了将Nod与减数分裂染色体结合外,可能还发挥其他作用。

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