LeGouy E, Thompson E M, Muchardt C, Renard J P
Unité de Biologie du Développement, Institut National de la Recherche Agronomique, Jouy en Josas, France.
Dev Dyn. 1998 May;212(1):38-48. doi: 10.1002/(SICI)1097-0177(199805)212:1<38::AID-AJA4>3.0.CO;2-3.
Epigenetic regulation of gene expression through modification of chromatin organization is an important mechanism in the development of eucaryotic organisms. We investigated the developmentally regulated expression of the mouse mBRG1 and mbrm genes, which are homologous to the yeast SWI2 gene. Both proteins are involved in chromatin remodeling as components of the mammalian SWI/SNF complex. The analysis was performed at a time in mouse development when the formation of a functional zygotic nucleus is closely linked to extensive chromatin modifications. Reverse transcription-polymerase chain reaction (RT-PCR) analysis in mature oocytes and through the first cleavage stages showed that both genes were highly expressed as maternal products but that they subsequently exhibited considerable differences in their level of expression when the transition to zygotic transcription occurred. Immunodetection of the two proteins with specific antibodies paralleled the RT-PCR analysis. The mBRG1 protein was present throughout preimplantation development, whereas zygotic mbrm was clearly detectable only when differentiation first occurs at the blastocyst stage. At this stage, mbrm was restricted to the inner cell mass. Cell type-specific expression of mbrm was also observed after in vitro differentiation of embryonic stem cells. These results indicate that the two murine homologues of SWI2 have substantially different roles in chromatin organization during the onset of embryonic development.
通过染色质组织修饰对基因表达进行表观遗传调控是真核生物发育过程中的一种重要机制。我们研究了小鼠mBRG1和mbrm基因的发育调控表达,它们与酵母SWI2基因同源。这两种蛋白质作为哺乳动物SWI/SNF复合物的组成部分参与染色质重塑。分析是在小鼠发育的一个阶段进行的,此时功能性合子核的形成与广泛的染色质修饰密切相关。对成熟卵母细胞和第一次卵裂阶段进行的逆转录-聚合酶链反应(RT-PCR)分析表明,这两个基因作为母源产物均高度表达,但在向合子转录转变时,它们随后的表达水平表现出相当大的差异。用特异性抗体对这两种蛋白质进行免疫检测与RT-PCR分析结果一致。mBRG1蛋白在整个着床前发育过程中都存在,而合子型mbrm仅在囊胚阶段首次出现分化时才能清晰检测到。在此阶段,mbrm仅限于内细胞团。在胚胎干细胞体外分化后也观察到了mbrm的细胞类型特异性表达。这些结果表明,SWI2的两个小鼠同源物在胚胎发育开始时的染色质组织中具有截然不同的作用。