EVOLUTION OF THE SNF2 FAMILY OF PROTEINS - SUBFAMILIES WITH DISTINCT SEQUENCES AND FUNCTIONS

被引:609
作者
EISEN, JA
SWEDER, KS
HANAWALT, PC
机构
[1] Department of Biological Sciences, Stanford University, Stanford
关键词
D O I
10.1093/nar/23.14.2715
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 SNF2 family of proteins includes representatives from a variety of species with roles in cellular processes such as transcriptional regulation (e.g, MOT1, SNF2 and BRM), maintenance of chromosome stability during mitosis (e.g. lodestar) and various aspects of processing of DNA damage, including nucleotide excision repair (e.g. RAD16 and ERCC6), recombinational pathways (e,g, RAD54) and post-replication daughter strand gap repair (e.g, RAD5), This family also includes many proteins with no known function, To better characterize this family of proteins we have used molecular phylogenetic techniques to infer evolutionary relationships among the family members, We have divided the SNF2 family into multiple subfamilies, each of which represents what we propose to be a functionally and evolutionarily distinct group, We have then used the subfamily structure to predict the functions of some of the uncharacterized proteins in the SNF2 family. We discuss possible implications of this evolutionary analysis on the general properties and evolution of the SNF2 family.
引用
收藏
页码:2715 / 2723
页数:9
相关论文
共 81 条
[71]  
TAMKUN JW, 1992, MOL CELL BIOL, V12, P1893
[72]   CLUSTAL-W - IMPROVING THE SENSITIVITY OF PROGRESSIVE MULTIPLE SEQUENCE ALIGNMENT THROUGH SEQUENCE WEIGHTING, POSITION-SPECIFIC GAP PENALTIES AND WEIGHT MATRIX CHOICE [J].
THOMPSON, JD ;
HIGGINS, DG ;
GIBSON, TJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (22) :4673-4680
[73]   ERCC6, A MEMBER OF A SUBFAMILY OF PUTATIVE HELICASES, IS INVOLVED IN COCKAYNES-SYNDROME AND PREFERENTIAL REPAIR OF ACTIVE GENES [J].
TROELSTRA, C ;
VANGOOL, A ;
DEWIT, J ;
VERMEULEN, W ;
BOOTSMA, D ;
HOEIJMAKERS, JHJ .
CELL, 1992, 71 (06) :939-953
[74]   THE SACCHAROMYCES-CEREVISIAE NPS1 GENE, A NOVEL CDC GENE WHICH ENCODES A 160 KDA NUCLEAR-PROTEIN INVOLVED IN G(2) PHASE-CONTROL [J].
TSUCHIYA, E ;
UNO, M ;
KIGUCHI, A ;
MASUOKA, K ;
KANEMORI, Y ;
OKABE, S ;
MIKAYAWA, T .
EMBO JOURNAL, 1992, 11 (11) :4017-4026
[75]   SEQUENCE-ANALYSIS OF A 31 KB DNA FRAGMENT FROM THE RIGHT ARM OF SACCHAROMYCES-CEREVISIAE CHROMOSOME-II [J].
VANDERAART, QJM ;
BARTHE, C ;
DOIGNON, F ;
AIGLE, M ;
CROUZET, M ;
STEENSMA, HY .
YEAST, 1994, 10 (07) :959-964
[76]   RAD26, THE FUNCTIONAL SACCHAROMYCES-CEREVISIAE HOMOLOG OF THE COCKAYNE-SYNDROME-B GENE ERCC6 [J].
VANGOOL, AJ ;
VERHAGE, R ;
SWAGEMAKERS, SMA ;
VANDEPUTTE, P ;
BROUWER, J ;
TROELSTRA, C ;
BOOTSMA, D ;
HOEIJMAKERS, JHJ .
EMBO JOURNAL, 1994, 13 (22) :5361-5369
[77]  
VENEMA J, 1991, MUTAT RES, V255, P123
[78]  
WILSON R, GI458966
[79]   TRANSCRIPTIONAL ACTIVATION - SWITCHED-ON CHROMATIN [J].
WOLFFE, AP .
CURRENT BIOLOGY, 1994, 4 (06) :525-528
[80]   THE GAM1/SNF2 GENE OF SACCHAROMYCES-CEREVISIAE ENCODES A HIGHLY CHARGED NUCLEAR-PROTEIN REQUIRED FOR TRANSCRIPTION OF THE STA1 GENE [J].
YOSHIMOTO, H ;
YAMASHITA, I .
MOLECULAR & GENERAL GENETICS, 1991, 228 (1-2) :270-280