Analysis of the yeast genome: Identification of new non-coding and small ORF-containing RNAs

被引:66
作者
Olivas, WM
Muhlrad, D
Parker, R
机构
[1] UNIV ARIZONA,DEPT MOL & CELLULAR BIOL,TUCSON,AZ 85721
[2] UNIV ARIZONA,HOWARD HUGHES MED INST,TUCSON,AZ 85721
关键词
D O I
10.1093/nar/25.22.4619
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The genome sequences from increasing numbers of organisms allow for rapid and organized examination of gene expression. Yet current computational-based paradigms for gene recognition are limited and likely to miss genes expressing non-coding RNAs or mRNAs with small open reading frames (ORFs). We have utilized two strategies to determine if there are additional transcripts in the yeast Saccharomyces cerevisiae that were not identified in previous analyses of the genome, In one approach, we identified strong consensus polymerase III promoters based on sequence, and determined experimentally if these promoters drive the expression of an RNA polymerase III transcript. This approach led to the identification of a new, non-essential 170 nt non-coding RNA. An alternative strategy analyzed RNA expression from large sequence gaps >2 kb between predicted ORFs. Fifteen unique RNA transcripts ranging in size from 161 to 1200 nt were identified from a total of 59 sequence gaps. Several of these RNAs contain unusually small potential ORFs, while one is clearly non-coding and appears to be a small nucleolar RNA. These results suggest that there are likely to be additional previously unidentified non-coding RNAs in yeast, and that new paradigms for gene recognition will be required to identify all expressed genes from an organism.
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收藏
页码:4619 / 4625
页数:7
相关论文
共 37 条
[1]  
Ausubel FM, 1995, CURRENT PROTOCOLS MO
[2]   ANTISENSE SNORNAS - A FAMILY OF NUCLEOLAR RNAS WITH LONG COMPLEMENTARITIES TO RIBOSOMAL-RNA [J].
BACHELLERIE, JP ;
MICHOT, B ;
NICOLOSO, M ;
BALAKIN, A ;
NI, JW ;
FOURNIER, MJ .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (07) :261-264
[3]   The RNA world of the nucleolus: Two major families of small RNAs defined by different box elements with related functions [J].
Balakin, AG ;
Smith, L ;
Fournier, MJ .
CELL, 1996, 86 (05) :823-834
[4]   A SUPPRESSOR OF TBP MUTATIONS ENCODES AN RNA POLYMERASE-III TRANSCRIPTION FACTOR WITH HOMOLOGY TO TFIIB [J].
BURATOWSKI, S ;
ZHOU, H .
CELL, 1992, 71 (02) :221-230
[5]   A SMALL SEGMENT OF THE MAT-ALPHA-1 TRANSCRIPT PROMOTES MESSENGER-RNA DECAY IN SACCHAROMYCES-CEREVISIAE - A STIMULATORY ROLE FOR RARE CODONS [J].
CAPONIGRO, G ;
MUHLRAD, D ;
PARKER, R .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (09) :5141-5148
[6]   MULTIFUNCTIONAL YEAST HIGH-COPY-NUMBER SHUTTLE VECTORS [J].
CHRISTIANSON, TW ;
SIKORSKI, RS ;
DANTE, M ;
SHERO, JH ;
HIETER, P .
GENE, 1992, 110 (01) :119-122
[7]   REGULATION OF GENE-EXPRESSION BY TRANS-ENCODED ANTISENSE RNAS [J].
DELIHAS, N .
MOLECULAR MICROBIOLOGY, 1995, 15 (03) :411-414
[8]   HERPESVIRUS SAIMIRI SMALL RNA AND INTERLEUKIN-4 MESSENGER-RNA AUUUA REPEATS COMPETE FOR SEQUENCE-SPECIFIC FACTORS INCLUDING A NOVEL 70K PROTEIN [J].
GECK, P ;
MEDVECZKY, MM ;
CHOU, CS ;
BROWN, A ;
CUS, J ;
MEDVECZKY, PG .
JOURNAL OF GENERAL VIROLOGY, 1994, 75 :2293-2301
[9]   TRANSCRIPTION BY RNA POLYMERASE-III [J].
GEIDUSCHEK, EP ;
TOCCHINIVALENTINI, GP .
ANNUAL REVIEW OF BIOCHEMISTRY, 1988, 57 :873-914
[10]  
Gietz RD, 1995, METHOD MOL CELL BIOL, V5, P255