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Role of the snRNAs in spliceosomal active site

Journal

RNA BIOLOGY
Volume 7, Issue 3, Pages 345-353

Publisher

TAYLOR & FRANCIS INC
DOI: 10.4161/rna.7.3.12089

Keywords

spliceosome; ribozyme; U6; U2; snRNAs; catalysis; splicing; RNA world

Funding

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM078572] Funding Source: NIH RePORTER
  2. NIGMS NIH HHS [R01 GM078572] Funding Source: Medline

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The spliceosome, the ribonucleoprotein assembly that removes the intervening sequences from pre-mRNAs through splicing, is one of the most complex cellular machines. In humans it is composed of similar to 150 proteins and five RNAs (snRNAs). One of the snRNAs, U6, contains sequences analogous to all the RNA elements that form the active site of the group II introns, ribozymes that perform a splicing reaction mechanistically identical to spliceosomal splicing. Interestingly, U6 is the only snRNA that is indispensable for splicing and in vitro, in complex with another snRNA, it can catalyze a primordial splicing reaction in the absence of all other spliceosomal factors. On the other hand, discovery of an RNase H-like domain in a spliceosomal protein that is closely associated with splice sites suggests that proteins may be involved in formation of the active site. Thus, whether the spliceosome is an RNA or RNA-protein catalyst remains uncertain.

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