Caenorhabditis elegans mRNAs that encode a protein similar to ADARs derivefrom an operon containing six genes

Citation
Rf. Hough et al., Caenorhabditis elegans mRNAs that encode a protein similar to ADARs derivefrom an operon containing six genes, NUCL ACID R, 27(17), 1999, pp. 3424-3432
Citations number
41
Categorie Soggetti
Biochemistry & Biophysics
Journal title
NUCLEIC ACIDS RESEARCH
ISSN journal
03051048 → ACNP
Volume
27
Issue
17
Year of publication
1999
Pages
3424 - 3432
Database
ISI
SICI code
0305-1048(19990901)27:17<3424:CEMTEA>2.0.ZU;2-R
Abstract
The Caenorhabditis elegans T20H4.4 open reading frame (GenBank accession no , U00037) predicted by Genefinder encodes a 367 amino acid protein that is 32-35% identical to the C-terminal domain of adenosine deaminases that act on RNA, We show that T20H4.4 cDNAs (GenBank accession no. AF051275) encode a larger 495 amino acid protein that is extended at its N-terminus to inclu de a single double-stranded RNA-binding motif, and that T20H4.4 occupies th e second position in a six-gene operon (5'-T20H4.5, T20H4.4, R151.8A, R151. 8B, R151.7, R151.6-3'), Ten different spliced-leader (SL) sequences were fo und attached to T20H4.4 mRNAs, including SL1, SL2 and eight SL2-like leader s that include two new variants. Characterization of cDNAs derived from all six genes confirmed the essential features of C. elegans operons: intercis tronic distances in the range of 104-257 nt between the upstream polyadenyl ation sites and the downstream trans-splice sites; SL2, or SL2-like leaders , attached to the downstream mRNAs. Polycistronic mRNA fragments revealed a 5'-untranslated region (5'-UTR) >705 nt, The 5'-UTR is removed in mature m RNAs from the first gene (T20H4.5) and replaced primarily by SL1, and to a lesser extent by SL2. Our study provides new information regarding operons and how they are processed.