Hostname: page-component-586b7cd67f-gb8f7 Total loading time: 0 Render date: 2024-11-27T22:13:06.342Z Has data issue: false hasContentIssue false

Identification of the gene encoding the 5S ribosomal RNA maturase in Bacillus subtilis: Mature 5S rRNA is dispensable for ribosome function

Published online by Cambridge University Press:  07 February 2001

CIARÁN CONDON
Affiliation:
Unité Propre de Recherche 9073, Institut de Biologie Physico-Chimique, 75005 Paris, France
DOMINIQUE BRECHEMIER-BAEY
Affiliation:
Unité Propre de Recherche 9073, Institut de Biologie Physico-Chimique, 75005 Paris, France
BELTCHO BELTCHEV
Affiliation:
Unité Propre de Recherche 9073, Institut de Biologie Physico-Chimique, 75005 Paris, France
MARIANNE GRUNBERG-MANAGO
Affiliation:
Unité Propre de Recherche 9073, Institut de Biologie Physico-Chimique, 75005 Paris, France
HARALD PUTZER
Affiliation:
Unité Propre de Recherche 9073, Institut de Biologie Physico-Chimique, 75005 Paris, France
Get access

Abstract

Over 25 years ago, Pace and coworkers described an activity called RNase M5 in Bacillus subtilis cell extracts responsible for 5S ribosomal RNA maturation (Sogin & Pace, Nature, 1974, 252:598–600). Here we show that RNase M5 is encoded by a gene of previously unknown function that is highly conserved among the low G + C Gram-positive bacteria. We propose that the gene be named rnmV. The rnmV gene is nonessential. B. subtilis strains lacking RNase M5 do not make mature 5S rRNA, indicating that this process is not necessary for ribosome function. 5S rRNA precursors can, however, be found in both free and translating ribosomes. In contrast to RNase E, which cleaves the Escherichia coli 5S precursor in a single-stranded region, which is then trimmed to yield mature 5S RNA, RNase M5 cleaves the B. subtilis equivalent in a double-stranded region to yield mature 5S rRNA in one step. For the most part, eubacteria contain one or the other system for 5S rRNA production, with an imperfect division along Gram-negative and Gram-positive lines. A potential correlation between the presence of RNase E or RNase M5 and the single- or double-stranded nature of the predicted cleavage sites is explored.

Type
Research Article
Copyright
2001 RNA Society

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)