Kadowaki T, Chen S, Hitomi M, Jacobs E, Kumagai C, Liang S, Schneiter R, Singleton D, Wisniewska J, Tartakoff A M
Institute of Pathology, Case Western Reserve University, Cleveland, Ohio 44106.
J Cell Biol. 1994 Aug;126(3):649-59. doi: 10.1083/jcb.126.3.649.
To understand the mechanisms of mRNA transport in eukaryotes, we have isolated Saccharomyces cerevisiae temperature-sensitive (ts) mutants which accumulate poly(A)+ RNA in the nucleus at the restrictive temperature. A total of 21 recessive mutants were isolated and classified into 16 complementation groups. Backcrossed mRNA transport-defective strains from each complementation group have been analyzed. A strain which is ts for heat shock transcription factor was also analyzed since it also shows nuclear accumulation of poly(A)+ RNA at 37 degrees C. At 37 degrees C the mRNA of each mutant is characterized by atypically long polyA tails. Unlike ts pre-mRNA splicing mutants, these strains do not interrupt splicing of pre-mRNA at 37 degrees C; however four strains accumulate oversized RNA polymerase II transcripts. Some show inhibition of rRNA processing and a further subset of these strains is also characterized by inhibition of tRNA maturation. Several strains accumulate nuclear proteins in the cytoplasm when incubated at semipermissive temperature. Remarkably, many strains exhibit nucleolar fragmentation or enlargement at the restrictive temperature. Most strains show dramatic ultrastructural alterations of the nucleoplasm or nuclear membrane. Distinct mutants accumulate poly(A)+ RNA in characteristic patterns in the nucleus.
为了解真核生物中mRNA转运的机制,我们分离了酿酒酵母温度敏感(ts)突变体,这些突变体在限制温度下会在细胞核中积累多聚腺苷酸(poly(A)+)RNA。总共分离出21个隐性突变体,并将其分为16个互补组。对来自每个互补组的回交mRNA转运缺陷菌株进行了分析。由于热休克转录因子温度敏感的菌株在37℃时也表现出多聚腺苷酸(poly(A)+)RNA的核内积累,因此也对其进行了分析。在37℃时,每个突变体的mRNA都具有异常长的多聚腺苷酸尾巴。与温度敏感的前体mRNA剪接突变体不同,这些菌株在37℃时不会中断前体mRNA的剪接;然而,有四个菌株积累了超大的RNA聚合酶II转录本。一些菌株表现出rRNA加工的抑制,并且这些菌株的一个进一步子集还具有tRNA成熟抑制的特征。当在半允许温度下培养时,几个菌株在细胞质中积累核蛋白。值得注意的是,许多菌株在限制温度下表现出核仁碎片化或增大。大多数菌株显示核质或核膜有明显的超微结构改变。不同的突变体在细胞核中以特征性模式积累多聚腺苷酸(poly(A)+)RNA。