Hostname: page-component-cd9895bd7-gvvz8 Total loading time: 0 Render date: 2024-12-28T16:36:27.139Z Has data issue: false hasContentIssue false

Translation during cold adaptation does not involve mRNA–rRNA base pairing through the downstream box

Published online by Cambridge University Press:  31 October 2000

ANNA LA TEANA
Affiliation:
Istituto di Biochimica, Università di Ancona, 60131 Ancona, Italy
ANNA BRANDI
Affiliation:
Dipartimento di Biologia MCA, Università di Camerino, 62032 Camerino (MC), Italy
MICHAEL O'CONNOR
Affiliation:
J.W. Wilson Laboratory, Department of Molecular and Cellular Biology and Biochemistry, Brown University, Providence, Rhode Island 02912, USA
SIMONA FREDDI
Affiliation:
Istituto di Biochimica, Università di Ancona, 60131 Ancona, Italy
CYNTHIA L. PON
Affiliation:
Dipartimento di Biologia MCA, Università di Camerino, 62032 Camerino (MC), Italy
Get access

Abstract

The downstream box (DB) has been proposed to enhance translation of several mRNAs and to be a key element controlling the expression of cold-shocked mRNAs. However, the proposal that the DB exerts its effects through a base pairing interaction with the complementary anti-downstream box (antiDB) sequence (nt 1469–1483) located in the penultimate stem (helix 44) of 16S rRNA remains controversial. The existence of this interaction during initiation of protein synthesis under cold-shock conditions has been investigated in the present work using an Escherichia coli strain whose ribosomes lack the potential to base pair with mRNA because of a 12 bp inversion of the antiDB sequence in helix 44. Our results show that this strain is capable of cold acclimation, withstands cold shock, and its ribosomes translate mRNAs that contain or lack DB sequences with similar efficiency, comparable to that of the wild type. The structure of helix 44 in 30S ribosomal subunits from cells grown at 37 °C and from cells subjected to cold shock was also analyzed by binding a 32P-labeled oligonucleotide complementary to the antiDB region and by chemical probing with DMS and kethoxal. Both approaches clearly indicate that this region is in a double-stranded conformation and therefore not available for base pairing with mRNA.

Type
Research Article
Copyright
2000 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.)