Conserved features of Y RNAs revealed by automated phylogenetic secondary structure analysis

被引:28
作者
Farris, AD
Koelsch, G
Pruijn, GJM
van Venrooij, WJ
Harley, JB
机构
[1] Oklahoma Med Res Fdn, Oklahoma City, OK 73104 USA
[2] Univ Nijmegen, Dept Biochem, Nijmegen, Netherlands
关键词
D O I
10.1093/nar/27.4.1070
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
Y RNAs are small 'cytoplasmic' RNAs which are components of the Ro ribonucleoprotein (RNP) complex. The core of this complex, which is found in the cell nuclei of higher eukaryotes as well as the cytoplasm, is composed of a complex between the 60 kDa Ro protein and Y RNAs, Human cells contain four distinct Y RNAs (Y1, Y3, Y4 and Y5), while other eukaryotes contain a variable number of Y RNA homologues, When detected in a particular species, the Ro RNP has been present in every cell type within that particular organism. This characteristic, along with its high conservation among vertebrates, suggests an important function for Ro RNP in cellular metabolism; however, this function has not yet been definitively elucidated. In order to identify conserved features of Y RNA sequences and structures which may be directly involved in Ro RNP function, a phylogenetic comparative analysis of Y RNAs has been performed. Sequences of Y RNA homologues from five vertebrate species have been obtained and, together with previously published Y RNA sequences, used to predict Y RNA secondary structures. A novel RNA secondary structure comparison algorithm, the suboptimal RNA analysis program, has been developed and used in conjunction with available algorithms to find phylogenetically conserved secondary structure models for Y1, Y3 and Y4 RNAs, Short, conserved sequences within the Y RNAs have been identified and are invariant among vertebrates, consistent with a direct role for Y RNAs in Ro function, A subset of these are located wholly or partially in looped regions in the Y3 and Y4 RNA predicted model structures, in accord with the possibility that these Y RNAs base pair with other cellular nucleic acids or are sites of interaction between the Ro RNP and other macromolecules.
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页码:1070 / 1078
页数:9
相关论文
共 42 条
[1]   ISOLATION AND CHARACTERIZATION OF A CDNA CLONE ENCODING THE 60-KD COMPONENT OF THE HUMAN SS-A/RO RIBONUCLEOPROTEIN AUTO-ANTIGEN [J].
BENCHETRIT, E ;
GANDY, BJ ;
TAN, EM ;
SULLIVAN, KF .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (04) :1284-1292
[2]   HUMAN RO RIBONUCLEOPROTEIN-PARTICLES - CHARACTERIZATION OF NATIVE STRUCTURE AND STABLE ASSOCIATION WITH THE LA POLYPEPTIDE [J].
BOIRE, G ;
CRAFT, J .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (04) :1182-1190
[3]   SNRNPS AND SCRNPS AS AUTOANTIGENS - CLUES TO THE ETIOLOGY OF THE CONNECTIVE-TISSUE DISEASES [J].
CRAFT, J ;
MAMULA, M ;
OHOSONE, Y ;
BOIRE, G ;
GOLD, H ;
HARDIN, J .
CLINICAL RHEUMATOLOGY, 1990, 9 (01) :10-18
[4]   GENETIC-EVIDENCE FOR BASE-PAIRING BETWEEN U2 AND U6 SNRNA IN MAMMALIAN MESSENGER-RNA SPLICING [J].
DATTA, B ;
WEINER, AM .
NATURE, 1991, 352 (6338) :821-824
[5]   MOLECULAR ANALYSIS OF THE 60-KDA HUMAN RO RIBONUCLEOPROTEIN [J].
DEUTSCHER, SL ;
HARLEY, JB ;
KEENE, JD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (24) :9479-9483
[6]  
DEVEREUX J, 1989, GCG SEQUENCE ANAL SO
[7]   Genes for murine Y1 and Y3 Ro RNAs have class 3 RNA polymerase III promoter structures and are unlinked on mouse chromosome 6 [J].
Farris, AD ;
Gross, JK ;
Hanas, JS ;
Harley, JB .
GENE, 1996, 174 (01) :35-42
[8]   The ultrastructural localization of 60-kDa Ro protein and human cytoplasmic RNAs: Association with novel electron-dense bodies [J].
Farris, AD ;
PuvionDutilleul, F ;
Puvion, E ;
Harley, JB ;
Lee, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) :3040-3045
[9]   Y3 IS THE MOST CONSERVED SMALL RNA COMPONENT OF RO RIBONUCLEOPROTEIN COMPLEXES IN VERTEBRATE SPECIES [J].
FARRIS, AD ;
OBRIEN, CA ;
HARLEY, JB .
GENE, 1995, 154 (02) :193-198
[10]  
FARRIS AD, 1995, THESIS U OKLAHOMA OK, P113