RNomics:: an experimental approach that identifies 201 candidates for novel, small, non-messenger RNAs in mouse

被引:258
作者
Hüttenhofer, A [1 ]
Kiefmann, M
Meier-Ewert, S
O'Brien, J
Lehrach, H
Bachellerie, JP
Brosius, J
机构
[1] ZMBE, Inst Expt Pathol Mol Neurobiol, D-48149 Munster, Germany
[2] Max Planck Inst Mol Genet, D-14195 Berlin, Germany
[3] Univ Toulouse 3, Lab Biol Mol Eucaryote, CNRS, F-31062 Toulouse, France
关键词
cDNA library; non-messenger RNAs; RNomics; snoRNAs;
D O I
10.1093/emboj/20.11.2943
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
In mouse brain cDNA libraries generated from small RNA molecules we have identified a total of 201 different expressed RNA sequences potentially encoding novel small non-messenger RNA species (snmRNAs), Based on sequence and structural motifs, 113 of these RNAs can be assigned to the C/D box or H/ACA box subclass of small nucleolar RNAs (snoRNAs), known as guide RNAs for rRNA, While 30 RNAs represent mouse homologues of previously identified human CCD or H/ACA snoRNAs, 83 correspond to entirely novel snoRNAs, Among these, for the first time, we identified four C/D box snoRNAs and four H/ACA box snoRNAs predicted to direct modifications within U2, U4 or U6 small nuclear RNAs (snRNAs), Furthermore, 25 snoRNAs from either class lacked antisense elements for rRNAs or snRNAs, Therefore, additional snoRNA targets have to be considered, Surprisingly, six C/D box snoRNAs and one H/ACA box snoRNA were expressed exclusively in brain. Of the 88 RNAs not belonging to either snoRNA subclass, at least 26 are probably derived from truncated heterogeneous nuclear RNAs (hnRNAs) or mRNAs, Short interspersed repetitive elements (SINEs) are located on five RNA sequences and may represent rare examples of transcribed SINEs, The remaining RNA species could not as yet be assigned either to any snmRNA class or to a part of a larger hnRNA/mRNA, It is likely that at least some of the latter will represent novel, unclassified snmRNAs.
引用
收藏
页码:2943 / 2953
页数:11
相关论文
共 46 条
[31]  
Ofengand J., 1998, Modification and editing of RNA, P229
[32]  
OLIVAS WM, 1997, NUCLEIC ACIDS RES, V22, P4619
[33]   The plurifunctional nucleolus [J].
Pederson, T .
NUCLEIC ACIDS RESEARCH, 1998, 26 (17) :3871-3876
[34]   The host gene for intronic U17 small nucleolar RNAs in mammals has no protein-coding potential and is a member of the 5′-terminal oligopyrimidine gene family [J].
Pelczar, P ;
Filipowicz, W .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (08) :4509-4518
[35]   Human H/ACA small nucleolar RNPs and telomerase share evolutionarily conserved proteins NHP2 and NOP10 [J].
Pogacic, V ;
Dragon, F ;
Filipowicz, W .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (23) :9028-9040
[36]  
Qu LH, 1999, MOL CELL BIOL, V19, P1144
[37]   The role of oocyte transcription, the 5′UTR, and translation repression and derepression in Drosophila gurken mRNA and protein localization [J].
Saunders, C ;
Cohen, RS .
MOLECULAR CELL, 1999, 3 (01) :43-54
[38]  
Schmitt A.O., 1999, PCR APPL PROTOCOLS F, P457
[39]   Miranda mediates asymmetric protein and RNA localization in the developing nervous system [J].
Schuldt, AJ ;
Adams, JHJ ;
Davidson, CM ;
Micklem, DR ;
Haseloff, J ;
St Johnston, D ;
Brand, AH .
GENES & DEVELOPMENT, 1998, 12 (12) :1847-1857
[40]   Classification of gas5 as a multi-small-nucleolar-RNA (snoRNA) host gene and a member of the 5′-terminal oligopyrimidine gene family reveals common features of snoRNA host genes [J].
Smith, CM ;
Steitz, JA .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (12) :6897-6909