Cizdziel P E, de Mars M, Murphy E C
Department of Tumor Biology, University of Texas System Cancer Center, M.D. Anderson Hospital and Tumor Institute, Houston 77030.
Mol Cell Biol. 1988 Apr;8(4):1558-69. doi: 10.1128/mcb.8.4.1558-1569.1988.
The spliced form of MuSVts110 viral RNA is approximately 20-fold more abundant at growth temperatures of 33 degrees C or lower than at 37 to 41 degrees C. This difference is due to changes in the efficiency of MuSVts110 RNA splicing rather than selective thermolability of the spliced species at 37 to 41 degrees C or general thermosensitivity of RNA splicing in MuSVts110-infected cells. Moreover, RNA transcribed from MuSVts110 DNA introduced into a variety of cell lines is spliced in a temperature-sensitive fashion, suggesting that the structure of the viral RNA controls the efficiency of the event. We exploited this novel splicing event to study the cleavage and ligation events during splicing in vivo. No spliced viral mRNA or splicing intermediates were observed in MuSVts110-infected cells (6m2 cells) at 39 degrees C. However, after a short (about 30-min) lag following a shift to 33 degrees C, viral pre-mRNA cleaved at the 5' splice site began to accumulate. Ligated exons were not detected until about 60 min following the initial detection of cleavage at the 5' splice site, suggesting that these two splicing reactions did not occur concurrently. Splicing of viral RNA in the MuSVts110 revertant 54-5A4, which lacks the sequence -AG/TGT- at the usual 3' splice site, was studied. Cleavage at the 5' splice site in the revertant viral RNA proceeded in a temperature-sensitive fashion. No novel cryptic 3' splice sites were activated; however, splicing at an alternate upstream 3' splice site used at low efficiency in normal MuSVts110 RNA was increased to a level close to that of 5'-splice-site cleavage in the revertant viral RNA. Increased splicing at this site in 54-5A4 viral RNA is probably driven by the unavailability of the usual 3' splice site for exon ligation. The thermosensitivity of this alternate splice event suggests that the sequences governing the thermodependence of MuSVts110 RNA splicing do not involve any particular 3' splice site or branch point sequence, but rather lie near the 5' end of the intron.
MuSVts110病毒RNA的剪接形式在33℃或更低的生长温度下的丰度比在37至41℃时高约20倍。这种差异是由于MuSVts110 RNA剪接效率的变化,而不是剪接产物在37至41℃时的选择性热不稳定性或MuSVts110感染细胞中RNA剪接的一般热敏感性。此外,导入多种细胞系的MuSVts110 DNA转录的RNA以温度敏感的方式进行剪接,这表明病毒RNA的结构控制了该事件的效率。我们利用这种新的剪接事件来研究体内剪接过程中的切割和连接事件。在39℃时,在MuSVts110感染的细胞(6m2细胞)中未观察到剪接的病毒mRNA或剪接中间体。然而,在转移到33℃后经过短暂(约30分钟)的延迟,在5'剪接位点切割的病毒前体mRNA开始积累。直到在5'剪接位点最初检测到切割后约60分钟才检测到连接的外显子,这表明这两个剪接反应不是同时发生的。研究了MuSVts110回复株54-5A4中病毒RNA的剪接,该回复株在通常的3'剪接位点缺乏-AG/TGT-序列。回复株病毒RNA在5'剪接位点的切割以温度敏感的方式进行。没有激活新的隐蔽3'剪接位点;然而,在正常MuSVts110 RNA中低效率使用的另一个上游3'剪接位点的剪接增加到接近回复株病毒RNA中5'-剪接位点切割的水平。54-5A4病毒RNA中该位点剪接的增加可能是由于通常的3'剪接位点不可用于外显子连接。这种替代剪接事件的热敏感性表明,控制MuSVts110 RNA剪接热依赖性的序列不涉及任何特定的3'剪接位点或分支点序列,而是位于内含子的5'端附近。