Miriami E, Sperling J, Sperling R
Department of Genetics, Hebrew University of Jerusalem, Givat Ram, Israel.
Nucleic Acids Res. 1994 Aug 11;22(15):3084-91. doi: 10.1093/nar/22.15.3084.
The effect of heat shock on the packaging and splicing of nuclear CAD pre-mRNA, a transcript expressed constitutively from a non heat-inducible promoter, was studied in vivo in Syrian hamster cells. While mild heat shock did not affect significantly the packaging of CAD RNA in 200S InRNP particles, it caused perturbation to splicing. First, the heat shock inhibited splicing of CAD pre-mRNA. Second, it affected 5' splice site selection by activating cleavage at a cryptic 5' splice site; yet ligation of the cryptic exon to the downstream proximal exon was not observed. Base complementarities of the cryptic site with U1, U5, or U6 snRNAs are comparable, or even better, than those with the neighboring normal site. Hence, the exclusion of the cryptic site under normal growth conditions cannot be attributed to weaker base pairing with these snRNAs. On the other hand, these results imply the involvement of a heat labile factor in the selection of the 5' cleavage site. The exclusion of the cryptic site at 37 degrees C and the aborted splicing at this site after heat shock may also be explained by a proposed nuclear checking mechanism that detects in-frame stop codons upstream of the 5' splice site, and aborts splicing at such sites to prevent the production of a defective message.
在叙利亚仓鼠细胞中对热休克对核CAD前体mRNA(一种从非热诱导型启动子组成性表达的转录本)的包装和剪接的影响进行了体内研究。虽然轻度热休克对CAD RNA在200S InRNP颗粒中的包装没有显著影响,但它对剪接造成了干扰。首先,热休克抑制了CAD前体mRNA的剪接。其次,它通过激活一个隐蔽的5'剪接位点处的切割来影响5'剪接位点的选择;然而,未观察到隐蔽外显子与下游近端外显子的连接。隐蔽位点与U1、U5或U6 snRNA的碱基互补性与相邻正常位点的碱基互补性相当,甚至更好。因此,在正常生长条件下隐蔽位点的排除不能归因于与这些snRNA的碱基配对较弱。另一方面,这些结果意味着一种热不稳定因子参与了5'切割位点的选择。在37摄氏度时隐蔽位点的排除以及热休克后该位点剪接的中止也可以用一种提出的核检查机制来解释,该机制检测5'剪接位点上游的框内终止密码子,并在这些位点中止剪接以防止产生有缺陷的信息。