Spliceosomal small nuclear RNA genes in 11 insect genomes

被引:26
作者
Mount, Stephen M.
Gotea, Valer
Lin, Chiao-Feng
Hernandez, Kristina
Makalowski, Wojciech [1 ]
机构
[1] Penn State Univ, Mueller Lab 514, Inst Mol Evolut Genet, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Biol, University Pk, PA 16802 USA
[3] Penn State Univ, Dept Comp Sci & Engn, University Pk, PA 16802 USA
[4] Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA
[5] Univ Maryland, Ctr Bioinformat & Computat Biol, College Pk, MD 20742 USA
关键词
snRNA; spliceosomal snRNA; secondary structure; U12; introns; honeybee; Insecta;
D O I
10.1261/rna.259207
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 removal of introns from the primary transcripts of protein-coding genes is accomplished by the spliceosome, a large macromolecular complex of which small nuclear RNAs (snRNAs) are crucial components. Following the recent sequencing of the honeybee (Apis mellifera) genome, we used various computational methods, ranging from sequence similarity search to RNA secondary structure prediction, to search for putative snRNA genes (including their promoters) and to examine their pattern of conservation among 11 available insect genomes (A. mellifera, Tribolium castaneum, Bombyx mori, Anopheles gambiae, Aedes aegypti, and six Drosophila species). We identified candidates for all nine spliceosomal snRNA genes in all the analyzed genomes. All the species contain a similar number of snRNA genes, with the exception of A. aegypti, whose genome contains more U1, U2, and U5 genes, and A. mellifera, whose genome contains fewer U2 and U5 genes. We found that snRNA genes are generally more closely related to homologs within the same genus than to those in other genera. Promoter regions for all spliceosomal snRNA genes within each insect species share similar sequence motifs that are likely to correspond to the PSEA (proximal sequence element A), the binding site for snRNA activating protein complex, but these promoter elements vary in sequence among the five insect families surveyed here. In contrast to the other insect species investigated, Dipteran genomes are characterized by a rapid evolution (or loss) of components of the U12 spliceosome and a striking loss of U12-type introns.
引用
收藏
页码:5 / 14
页数:10
相关论文
共 41 条
[1]   The genome sequence of Drosophila melanogaster [J].
Adams, MD ;
Celniker, SE ;
Holt, RA ;
Evans, CA ;
Gocayne, JD ;
Amanatides, PG ;
Scherer, SE ;
Li, PW ;
Hoskins, RA ;
Galle, RF ;
George, RA ;
Lewis, SE ;
Richards, S ;
Ashburner, M ;
Henderson, SN ;
Sutton, GG ;
Wortman, JR ;
Yandell, MD ;
Zhang, Q ;
Chen, LX ;
Brandon, RC ;
Rogers, YHC ;
Blazej, RG ;
Champe, M ;
Pfeiffer, BD ;
Wan, KH ;
Doyle, C ;
Baxter, EG ;
Helt, G ;
Nelson, CR ;
Miklos, GLG ;
Abril, JF ;
Agbayani, A ;
An, HJ ;
Andrews-Pfannkoch, C ;
Baldwin, D ;
Ballew, RM ;
Basu, A ;
Baxendale, J ;
Bayraktaroglu, L ;
Beasley, EM ;
Beeson, KY ;
Benos, PV ;
Berman, BP ;
Bhandari, D ;
Bolshakov, S ;
Borkova, D ;
Botchan, MR ;
Bouck, J ;
Brokstein, P .
SCIENCE, 2000, 287 (5461) :2185-2195
[2]  
Bailey TL., 1994, P 2 INT C INT SYST M, V2, P28
[3]   Systematic genome-wide annotation of spliceosomal proteins reveals differential gene family expansion [J].
Barbosa-Morais, NL ;
Carmo-Fonseca, M ;
Aparício, S .
GENOME RESEARCH, 2006, 16 (01) :66-77
[4]   SPLICED SEGMENTS AT 5' TERMINUS OF ADENOVIRUS 2 LATE MESSENGER-RNA [J].
BERGET, SM ;
MOORE, C ;
SHARP, PA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (08) :3171-3175
[5]   Evolutionary fates and origins of U12-type introns [J].
Burge, CB ;
Padgett, RA ;
Sharp, PA .
MOLECULAR CELL, 1998, 2 (06) :773-785
[6]   Identification and analysis of U5 snRNA variants in Drosophila [J].
Chen, L ;
Lullo, DJ ;
Ma, EB ;
Celniker, SE ;
Rio, DC ;
Doudna, JA .
RNA, 2005, 11 (10) :1473-1477
[7]   AMAZING SEQUENCE ARRANGEMENT AT 5' ENDS OF ADENOVIRUS-2 MESSENGER-RNA [J].
CHOW, LT ;
GELINAS, RE ;
BROKER, TR ;
ROBERTS, RJ .
CELL, 1977, 12 (01) :1-8
[8]   WebLogo: A sequence logo generator [J].
Crooks, GE ;
Hon, G ;
Chandonia, JM ;
Brenner, SE .
GENOME RESEARCH, 2004, 14 (06) :1188-1190
[9]   Terminal intron dinucleotide sequences do not distinguish between U2- and U12-dependent introns [J].
Dietrich, RC ;
Incorvaia, R ;
Padgett, RA .
MOLECULAR CELL, 1997, 1 (01) :151-160
[10]   A memory-efficient dynamic programming algorithm for optimal alignment of a sequence to an RNA secondary structure [J].
Eddy, SR .
BMC BIOINFORMATICS, 2002, 3 (1)