Nelson D W, Honda B M
Department of Biological Sciences, Simon Fraser University, Burnaby, Canada.
Nucleic Acids Res. 1989 Nov 11;17(21):8657-67. doi: 10.1093/nar/17.21.8657.
The 5S RNA genes of Caenorhabditis briggsae consist of approximately 65 copies of a 1 kb repeat unit and 20 copies of a related 0.7 kb repeat unit, organized in separate tandem clusters. DNA sequence comparisons with the 1kb 5S DNA repeat from the closely related nematode C. elegans show that the 5S RNA coding region is perfectly conserved. Both C. briggsae 1 kb and 0.7 kb repeats are also efficiently transcribed in vitro,suggesting that both represent functional 5S RNA genes. Surprisingly, a second block of 118 bp is also perfectly conserved between the 1 kb repeats,and is less well conserved in the 0.7 kb repeat. In C. elegans, this DNA is transcribed to produce and abundant 100 nt transcript (SL RNA) which participates in a trans-splicing process (Krause and Hirsh, Cell 49:753, 1987). This SL RNA region of the C. briggsae 1 kb 5S DNA repeat also appears to be transcribed in vivo, while the corresponding region of the 0.7 kb repeat is not.
秀丽隐杆线虫的5S RNA基因由大约65个1 kb重复单元拷贝和20个相关的0.7 kb重复单元拷贝组成,它们分别组织成串联簇。与亲缘关系密切的线虫秀丽隐杆线虫的1 kb 5S DNA重复序列进行DNA序列比较表明,5S RNA编码区完全保守。秀丽隐杆线虫的1 kb和0.7 kb重复序列在体外也能高效转录,这表明它们都代表功能性5S RNA基因。令人惊讶的是,118 bp的第二个区域在1 kb重复序列之间也完全保守,而在0.7 kb重复序列中保守性较差。在秀丽隐杆线虫中,这段DNA被转录产生丰富的100 nt转录本(SL RNA),它参与反式剪接过程(克劳斯和赫什,《细胞》49:753,1987)。秀丽隐杆线虫1 kb 5S DNA重复序列的这个SL RNA区域在体内似乎也被转录,但0.7 kb重复序列的相应区域则不被转录。