RNase III cleaves eukaryotic preribosomal RNA at a U3 snoRNP-dependent site.

Abstract:

:A yeast gene homologous to bacterial RNase III (RNT1) encodes a double-strand-specific endoribonuclease essential for ribosome synthesis. Two rRNA processing events are blocked in cells temperature sensitive for RNT1: cleavage at the snoRNA-dependent AO site in the 5' ETS and cleavage in the 3' ETS. Recombinant RNT1 protein accurately cleaves a synthetic 5' ETS RNA at AO site in vitro, in the absence of snoRNA or other factors. A synthetic 3' ETS substrate is specifically cleaved at a site 21 nt downstream of the 3' end 28S rRNA. These observations show that a protein endonuclease collaborates with snoRNAs in eukaryotic rRNA processing and exclude a catalytic role for snoRNAs at certain pre-rRNA cleavage.

journal_name

Cell

journal_title

Cell

authors

Elela SA,Igel H,Ares M Jr

doi

10.1016/s0092-8674(00)81087-9

subject

Has Abstract

pub_date

1996-04-05 00:00:00

pages

115-24

issue

1

eissn

0092-8674

issn

1097-4172

pii

S0092-8674(00)81087-9

journal_volume

85

pub_type

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