Merker Robert J, Klein Hannah L
Department of Biochemistry and Kaplan Comprehensive Cancer Center, New York University School of Medicine, New York, New York 10016, USA.
Mol Cell Biol. 2002 Dec;22(24):8763-73. doi: 10.1128/MCB.22.24.8763-8773.2002.
The Saccharomyces cerevisiae hyperrecombination mutation hpr1Delta results in instability of sequences between direct repeats that is dependent on transcription of the repeat. Here it is shown that the HPR1 gene also functions in plasmid stability in the presence of destabilizing transcription elongation. In the hpr1Delta mutant, plasmid instability results from unchecked transcription elongation, which can be suppressed by a strong transcription terminator. The plasmid system has been used to examine in vivo aspects of transcription in the absence of Hpr1p. Nuclear run-on studies suggest that there is an increased RNA polymerase II density in the hpr1Delta mutant strain, but this is not accompanied by an increase in accumulation of cytoplasmic mRNA. Suppression of plasmid instability in hpr1Delta can also be achieved by high-copy expression of the RNA splicing factor SUB2, which has recently been proposed to function in mRNA export, in addition to its role in pre-mRNA splicing. High-copy-number SUB2 expression is accompanied by an increase in message accumulation from the plasmid, suggesting that the mechanism of suppression by Sub2p involves the formation of mature mRNA. Models for the role of Hpr1p in mature mRNA formation and the cause of plasmid instability in the absence of the Hpr1 protein are discussed.
酿酒酵母的高重组突变体hpr1Δ会导致同向重复序列之间的序列不稳定,这种不稳定依赖于重复序列的转录。本文表明,在存在不稳定转录延伸的情况下,HPR1基因在质粒稳定性方面也发挥作用。在hpr1Δ突变体中,质粒不稳定是由不受控制的转录延伸导致的,而这种延伸可被强转录终止子抑制。该质粒系统已被用于研究在缺乏Hpr1p的情况下转录的体内情况。细胞核连续标记研究表明,hpr1Δ突变体菌株中RNA聚合酶II的密度增加,但这并未伴随着细胞质mRNA积累的增加。RNA剪接因子SUB2的高拷贝表达也能抑制hpr1Δ中的质粒不稳定,最近有人提出SUB2除了在mRNA前体剪接中发挥作用外,还在mRNA输出中发挥作用。SUB2的高拷贝数表达伴随着质粒中信息积累的增加,这表明Sub2p的抑制机制涉及成熟mRNA的形成。文中讨论了Hpr1p在成熟mRNA形成中的作用模型以及在缺乏Hpr1蛋白时质粒不稳定的原因。