A genomewide search for ribozymes reveals an HDV-like sequence in the human CPEB3 gene

被引:213
作者
Salehi-Ashtiani, Kourosh
Luptak, Andrej
Litovchick, Alexander
Szostak, Jack W.
机构
[1] Massachusetts Gen Hosp, Dept Mol Biol, Howard Hughes Med Inst, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, CCIB, Simches Res Ctr 7215, Boston, MA 02114 USA
[3] Dana Farber Canc Inst, CCSB, Boston, MA 02115 USA
[4] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
关键词
HEPATITIS-DELTA-VIRUS; IN-VITRO SELECTION; SELF-CLEAVAGE; MESSENGER-RNA; NEURONAL ISOFORM; TRANSCRIPTION; CATALYSIS; SITE; HAMMERHEAD; EXPRESSION;
D O I
10.1126/science.1129308
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ribozymes are thought to have played a pivotal role in the early evolution of life, but relatively few have been identified in modern organisms. We performed an in vitro selection aimed at isolating self-cleaving RNAs from the human genome. The selection yielded several ribozymes, one of which is a conserved mammalian sequence that resides in an intron of the CPEB3 gene, which belongs to a family of genes regulating messenger RNA polyadenylation. The CPEB3 ribozyme is structurally and biochemically related to the human hepatitis delta virus (HDV) ribozymes. The occurrence of this ribozyme exclusively in mammals suggests that it may have evolved as recently as 200 million years ago. We postulate that HDV arose from the human transcriptome.
引用
收藏
页码:1788 / 1792
页数:5
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