Kadowaki T, Hitomi M, Chen S, Tartakoff A M
Institute of Pathology, Case Western Reserve University, Cleveland, Ohio 44106.
Mol Biol Cell. 1994 Nov;5(11):1253-63. doi: 10.1091/mbc.5.11.1253.
We have identified a set of genes that affect mRNA transport (mtr) from the nucleus to the cytoplasm of Saccharomyces cerevisiae. One of these genes, MTR2, has been cloned and shown to encode a novel 21-kDa nuclear protein that is essential for vegetative growth. MTR2 shows limited homology to a protein implicated in plasmid DNA transfer in Escherichia coli. PolyA+RNA accumulates within the nucleus of mtr2-1 in two to three foci at 37 degrees C. mRNA, tRNA, and rRNA synthesis continue as do pre-mRNA splicing, tRNA processing, and rRNA export at 37 degrees C. Under these conditions the polyA tail length increases, and protein synthesis is progressively inhibited. Nucleolar antigens also redistribute to two to three nuclear foci at 37 degrees C, and this redistribution depends on ongoing transcription by RNA polymerase II. Surprisingly, these foci coincide with the sites of polyA+RNA accumulation. Comparable colocalization and dependance on RNA polymerase II transcription is seen for the mtr1-1 mutant. The disorganization of the nucleolus thus depends on mRNA accumulation in these mutants. We discuss the possible functions of MTR2 and the yeast nucleolus in mRNA export.
我们已经鉴定出一组影响酿酒酵母mRNA从细胞核转运至细胞质的基因(mtr)。其中一个基因MTR2已被克隆,并显示其编码一种对营养生长至关重要的新型21kDa核蛋白。MTR2与一种参与大肠杆菌质粒DNA转移的蛋白具有有限的同源性。在37℃时,polyA + RNA在mtr2 - 1的细胞核内的两到三个位点积累。mRNA、tRNA和rRNA的合成在37℃时继续进行,前体mRNA剪接、tRNA加工和rRNA输出也是如此。在这些条件下,polyA尾长度增加,蛋白质合成逐渐受到抑制。核仁抗原在37℃时也重新分布到两到三个核位点,这种重新分布依赖于RNA聚合酶II的持续转录。令人惊讶的是,这些位点与polyA + RNA积累的位点重合。对于mtr1 - 1突变体,也观察到了类似的共定位以及对RNA聚合酶II转录的依赖性。因此,这些突变体中核仁的紊乱取决于mRNA的积累。我们讨论了MTR2和酵母核仁在mRNA输出中的可能功能。