Kadowaki T, Zhao Y, Tartakoff A M
Institute of Pathology, Case Western Reserve University, Cleveland, OH 44106.
Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2312-6. doi: 10.1073/pnas.89.6.2312.
Transport of mRNA from nucleus to cytoplasm is critical for eukaryotic gene expression; however, the mechanism of export is unknown. Selection and screening procedures have therefore been used to obtain a family of temperature-sensitive conditional mutants of Saccharomyces cerevisiae that accumulate poly(A)+ RNA in the nucleus when incubated at 37 degrees C, as judged by in situ hybridization. In one such mRNA transport mutant, mtr1-1, RNA synthesis continues, the export of poly(A)+ RNA is inhibited, intranuclear poly(A)+ is remarkably stable, and protein synthesis gradually stops. Thus, there is no tight coupling between RNA synthesis and export. The export lesion is reversible. Although mRNA export is clearly not a default option, neither inhibition of protein synthesis, inhibition of mRNA splicing, nor inhibition of poly(A)-binding protein function blocks export of the average poly(A)+, as judged by in situ hybridization. Further analysis of the family of mtr mutants should help map the path of RNA transport.
mRNA从细胞核转运到细胞质对于真核基因表达至关重要;然而,其输出机制尚不清楚。因此,人们采用了选择和筛选程序来获得酿酒酵母温度敏感型条件突变体家族,通过原位杂交判断,这些突变体在37℃孵育时会在细胞核中积累多聚腺苷酸(poly(A)+)RNA。在一个这样的mRNA转运突变体mtr1-1中,RNA合成继续进行,poly(A)+ RNA的输出受到抑制,核内poly(A)+非常稳定,蛋白质合成逐渐停止。因此,RNA合成与输出之间没有紧密的偶联。输出损伤是可逆的。尽管mRNA输出显然不是默认选项,但通过原位杂交判断,蛋白质合成抑制、mRNA剪接抑制或多聚腺苷酸结合蛋白功能抑制均不会阻断平均poly(A)+的输出。对mtr突变体家族的进一步分析应有助于绘制RNA转运途径。