Tejomurtula Jyothsna, Lee Kyung-Bon, Tripurani Swamy K, Smith George W, Yao Jianbo
Division of Animal and Nutritional Sciences, Laboratory of Animal Biotechnology and Genomics, West Virginia University, Morgantown, West Virginia 26506, USA.
Biol Reprod. 2009 Aug;81(2):333-42. doi: 10.1095/biolreprod.109.077396. Epub 2009 May 6.
Nuclear proteins such as transcription and chromatin remodeling factors are required for initiation of transcription in early embryos before embryonic genome activation. The nuclear transport of these proteins is mediated by transport factors such as importins. Through analysis of expressed sequence tags from a bovine oocyte cDNA library, we identified a new member of the importin alpha family (named importin alpha8). The cloned cDNA for bovine importin alpha8 (KPNA7) is 1817 base pair in length, encoding a protein of 522 amino acids that contains a conserved importin beta-binding domain and seven armadillo motifs. The RT-PCR analysis revealed that KPNA7 mRNA is specifically expressed in ovaries and mature oocytes. Real-time PCR demonstrated that KPNA7 expression in germinal vesicle (GV) oocytes is 33 to 2396 times higher than that of other importin alpha genes and that KPNA7 mRNA is abundant in GV and metaphase II oocytes, as well as in early-stage embryos collected before embryonic genome activation, but is barely detectable in morula- and blastocyst-stage embryos. Similarly, expression of KPNA7 protein is very high in oocytes and early embryos but is low in blastocysts. A glutathione S-transferase pull-down assay revealed that KPNA7 has a strong binding affinity for the nuclear protein nucleoplasmin 2 relative to that of other importin alphas. RNA interference experiments demonstrated that knockdown of KPNA7 in early embryos results in a decreased proportion of embryos developing to the blastocyst stage. These results suggest that KPNA7 may have an important role in the transport of essential nuclear proteins required for early embryogenesis.
在胚胎基因组激活之前,早期胚胎转录起始需要核蛋白,如转录和染色质重塑因子。这些蛋白质的核转运由输入蛋白等转运因子介导。通过分析牛卵母细胞cDNA文库的表达序列标签,我们鉴定出输入蛋白α家族的一个新成员(命名为输入蛋白α8)。克隆的牛输入蛋白α8(KPNA7)cDNA长度为1817个碱基对,编码一个由522个氨基酸组成的蛋白质,该蛋白质含有一个保守的输入蛋白β结合结构域和七个犰狳基序。RT-PCR分析显示,KPNA7 mRNA在卵巢和成熟卵母细胞中特异性表达。实时PCR表明,生发泡(GV)期卵母细胞中KPNA7的表达比其他输入蛋白α基因高33至2396倍,并且KPNA7 mRNA在GV期和中期II卵母细胞以及胚胎基因组激活前收集的早期胚胎中丰富,但在桑葚胚和囊胚期胚胎中几乎检测不到。同样,KPNA7蛋白的表达在卵母细胞和早期胚胎中非常高,但在囊胚中较低。谷胱甘肽S-转移酶下拉试验表明,相对于其他输入蛋白α,KPNA7与核蛋白核质素2具有很强的结合亲和力。RNA干扰实验表明,早期胚胎中KPNA7的敲低导致发育到囊胚期的胚胎比例降低。这些结果表明,KPNA7可能在早期胚胎发育所需的必需核蛋白的转运中起重要作用。