Tollervey D, Guthrie C
EMBO J. 1985 Dec 30;4(13B):3873-8. doi: 10.1002/j.1460-2075.1985.tb04160.x.
We have cloned and sequenced the single copy gene SNR10 which encodes the yeast small nuclear RNA, snR10. This species does not show obvious primary sequence homology to any previously identified small nuclear RNA. As an inital step towards determining the function of snR10, we have introduced insertions and deletions into the chromosomal copy of the gene. Strains lacking an intact copy of SNR10 are viable but considerably imparied in growth, particularly at elevated osmotic strengths or low temperatures; at 25 degrees C the doubling time of snr10- strains is 47% greater than that of otherwise isogenic SNR10 strains. As judged by the incorporation of radioactive precursors, snr10- strains are impaired in net RNA synthesis at low temperatures. The identification of a leaky, conditional phenotype associated with the deletion of this small nuclear RNA gene was entirely unexpected since the defect in snR10 synthesis is complete and non-conditional.
我们已经克隆并测序了编码酵母小核RNA(snR10)的单拷贝基因SNR10。该物种与任何先前鉴定的小核RNA均未显示出明显的一级序列同源性。作为确定snR10功能的第一步,我们已在该基因的染色体拷贝中引入了插入和缺失。缺乏完整SNR10拷贝的菌株是可行的,但生长受到相当大的损害,特别是在渗透压升高或低温下;在25℃时,snr10-菌株的倍增时间比其他同基因SNR10菌株长47%。通过放射性前体的掺入判断,snr10-菌株在低温下的净RNA合成受损。与该小核RNA基因缺失相关的渗漏性条件表型的鉴定完全出乎意料,因为snR10合成的缺陷是完全的且非条件性的。