A complete map of the human ribosomal protein genes: Assignment of 80 genes to the cytogenetic map and implications for human disorders

被引:110
作者
Uechi, T [1 ]
Tanaka, T [1 ]
Kenmochi, N [1 ]
机构
[1] Univ Ryukyus, Sch Med, Dept Biochem, Nishihara, Okinawa 9030215, Japan
基金
日本学术振兴会;
关键词
D O I
10.1006/geno.2000.6470
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Mapping of the human ribosomal protein (RP) genes has been completed, and all 80 different genes were placed on a cytogenetic map of the human genome. Because of the existence of processed pseudogenes, the localization of the RP genes was complicated, and five genes had remained to be mapped. Here we developed a novel strategy to identify sequence-tagged sites (STSs) at introns of the RP genes, and we localized RPL14 RPL22, RPL35, RPL36, and RPL39 within the chromosomes by radiation hybrid mapping. Unlike the case of eubacteria or archaebacteria, human RP genes are widely scattered about the genome. Together with the previous results, both sex chromosomes and 20 autosomes tall but chromosomes 7 and 21) were found to carry one or more RP genes. To explore the possible involvement of RP genes in human disorders, all 80 genes were assigned to cytogenetic bands according to a published cytogenetic BAC-STS map of the human genome. We compared the assigned positions with candidate regions for Mendelian disorders and found certain genes that might be involved in particular human disorders, (C) 2001 Academic Press.
引用
收藏
页码:223 / 230
页数:8
相关论文
共 39 条
[1]   NOONAN SYNDROME [J].
ALLANSON, JE .
JOURNAL OF MEDICAL GENETICS, 1987, 24 (01) :9-13
[2]  
AlMaghtheh M, 1996, AM J HUM GENET, V59, P864
[3]   AN INTEGRATED METRIC PHYSICAL MAP OF HUMAN-CHROMOSOME-19 [J].
ASHWORTH, LK ;
BATZER, MA ;
BRANDRIFF, B ;
BRANSCOMB, E ;
DEJONG, P ;
GARCIA, E ;
GARNES, JA ;
GORDON, LA ;
LAMERDIN, JE ;
LENNON, G ;
MOHRENWEISER, H ;
OLSEN, AS ;
SLEZAK, T ;
CARRANO, AV .
NATURE GENETICS, 1995, 11 (04) :422-427
[4]   Exploring the new world of the genome with DNA microarrays [J].
Brown, PO ;
Botstein, D .
NATURE GENETICS, 1999, 21 (Suppl 1) :33-37
[5]  
CRAMTON SE, 1994, GENETICS, V137, P1039
[6]  
Diamond L K, 1976, Adv Pediatr, V22, P349
[7]   The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia [J].
Draptchinskaia, N ;
Gustavsson, P ;
Andersson, B ;
Pettersson, M ;
Willig, TN ;
Dianzani, I ;
Ball, S ;
Tchernia, G ;
Klar, J ;
Matsson, H ;
Tentler, D ;
Mohandas, N ;
Carlsson, B ;
Dahl, N .
NATURE GENETICS, 1999, 21 (02) :169-175
[8]   NIGMS HUMAN RODENT SOMATIC-CELL HYBRID MAPPING PANEL-1 AND PANEL-2 [J].
DRWINGA, HL ;
TOJI, LH ;
KIM, CH ;
GREENE, AE ;
MULIVOR, RA .
GENOMICS, 1993, 16 (02) :311-314
[9]   HOMOLOGOUS RIBOSOMAL-PROTEIN GENES ON THE HUMAN X-CHROMOSOME AND Y-CHROMOSOME - ESCAPE FROM X-INACTIVATION AND POSSIBLE IMPLICATIONS FOR TURNER SYNDROME [J].
FISHER, EMC ;
BEERROMERO, P ;
BROWN, LG ;
RIDLEY, A ;
MCNEIL, JA ;
LAWRENCE, JB ;
WILLARD, HF ;
BIEBER, FR ;
PAGE, DC .
CELL, 1990, 63 (06) :1205-1218
[10]  
HALPERIN DS, 1989, BLOOD, V73, P1168