Ciejek E M, Nordstrom J L, Tsai M J, O'Malley B W
Biochemistry. 1982 Sep 28;21(20):4945-53. doi: 10.1021/bi00263a018.
Nuclear matrix was prepared by sequential treatment of oviduct nuclei with Triton X-100, DNase I, and 2 M NaCl. Published procedures were modified such that as many steps as possible were performed at -20 degrees C to minimize endogenous ribonuclease activity. Examination of electron micrographs confirmed the isolation of intact nuclear matrix structures. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis of the proteins in these structures showed an absence of histones and an enrichment of certain nonhistone proteins. RNA was isolated from the nuclear matrix preparations and subjected to denaturing gel electrophoresis. Gels were analyzed by ethidium bromide staining and by hybridization of Northern blots to cloned DNA probes for ovalbumin, ovomucoid, 5.8S ribosomal RNA, and U1 RNA. All of the precursors to ovalbumin and ovomucoid mRNAs (including various splicing intermediates) and all of the precursors to ribosomal RNA were associated exclusively with the nuclear matrix fraction. By contrast, mature ovalbumin and ovomucoid mRNAs were distributed between matrix and nonmatrix fractions. These observations were further supported by quantitative hybridization analysis of the RNA in nuclear and matrix fractions. It was found that less than 50% of the mature message of intact nuclei was recovered in the matrix, while most significantly, over 95% of the mRNA precursors remained associated with the matrix. Finally, mature ribosomal RNAs and virtually all of the small nuclear RNAs (including U1 RNA) were also distributed between matrix and nonmatrix fractions. Our results suggest that all precursor RNAs (be they precursors to mRNA or rRNA) are exclusively associated with the nuclear matrix and support the notion that the nuclear matrix may be the structural site for RNA processing within the nuclei of eucaryotic cells.
通过用Triton X-100、DNA酶I和2M NaCl依次处理输卵管细胞核来制备核基质。对已发表的实验步骤进行了修改,以便尽可能多的步骤在-20℃下进行,以尽量减少内源性核糖核酸酶的活性。电子显微镜检查证实了完整核基质结构的分离。对这些结构中的蛋白质进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳,结果显示没有组蛋白,某些非组蛋白得到了富集。从核基质制剂中分离出RNA,并进行变性凝胶电泳。通过溴化乙锭染色以及将Northern印迹与卵清蛋白、卵类粘蛋白、5.8S核糖体RNA和U1 RNA的克隆DNA探针杂交来分析凝胶。卵清蛋白和卵类粘蛋白mRNA的所有前体(包括各种剪接中间体)以及核糖体RNA的所有前体都仅与核基质部分相关。相比之下,成熟的卵清蛋白和卵类粘蛋白mRNA分布在基质和非基质部分之间。核部分和基质部分RNA的定量杂交分析进一步支持了这些观察结果。发现完整细胞核中不到50%的成熟信息在基质中回收,而最显著的是,超过95%的mRNA前体仍与基质相关。最后,成熟的核糖体RNA以及几乎所有的小核RNA(包括U1 RNA)也分布在基质和非基质部分之间。我们的结果表明,所有前体RNA(无论是mRNA还是rRNA的前体)都仅与核基质相关,并支持核基质可能是真核细胞细胞核内RNA加工的结构位点这一观点。