Characterization of DRP2, a novel human dystrophin homologue

被引:70
作者
Roberts, RG
Freeman, TC
Kendall, E
Vetrie, DLP
Dixon, AK
ShawSmith, C
Bone, Q
Bobrow, M
机构
[1] UMDS,DIV MED & MOLEC GENET,LONDON,ENGLAND
[2] ADDENBROOKES HOSP,DEPT MED GENET,CAMBRIDGE,ENGLAND
[3] SANGER CTR,HUMAN GENET GRP,HINXTON,ENGLAND
[4] HAMMERSMITH HOSP,GASTROENTEROL UNIT,LONDON,ENGLAND
[5] MARINE BIOL LAB,PLYMOUTH,DEVON,ENGLAND
关键词
D O I
10.1038/ng0696-223
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The currently recognised dystrophin protein family comprises the archetype, dystrophin, its close relative, utrophin or dystrophin-related protein (DRP), and a distantly related protein known as the 87K tyrosine kinase substrate. During the course of a phylogenetic study of sequences encoding the characteristic C-terminal domains of dystrophin-related proteins, we identified an unexpected novel class of vertebrate dystrophin- related sequences. We term this class dystrophin-related protein 2 (DRP2), and suggest that utrophin/DRP be renamed DRP1 to simplify future nomenclature. DRP2 is a relatively small protein, encoded in man by a 45 kb gene localized to Xq22. It is expressed principally in the brain and spinal cord, and is similar in overall structure to the Dp116 dystrophin isoform. The discovery of a novel relative of dystrophin substantially broadens the scope for study of this interesting group of proteins and their associated glycoprotein complexes.
引用
收藏
页码:223 / 226
页数:4
相关论文
共 24 条
  • [1] AN ALTERNATIVE DYSTROPHIN TRANSCRIPT SPECIFIC TO PERIPHERAL-NERVE
    BYERS, TJ
    LIDOV, HGW
    KUNKEL, LM
    [J]. NATURE GENETICS, 1993, 4 (01) : 77 - 81
  • [2] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [3] ALTERNATIVE SPLICING OF HUMAN DYSTROPHIN MESSENGER-RNA GENERATES ISOFORMS AT THE CARBOXY TERMINUS
    FEENER, CA
    KOENIG, M
    KUNKEL, LM
    [J]. NATURE, 1989, 338 (6215) : 509 - 511
  • [4] RAPID PRODUCTION OF FULL-LENGTH CDNAS FROM RARE TRANSCRIPTS - AMPLIFICATION USING A SINGLE GENE-SPECIFIC OLIGONUCLEOTIDE PRIMER
    FROHMAN, MA
    DUSH, MK
    MARTIN, GR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) : 8998 - 9002
  • [5] MOLECULAR PATHOLOGY OF HAEMOPHILIA-B
    GREEN, PM
    BENTLEY, DR
    MIBASHAN, RS
    NILSSON, IM
    GIANNELLI, F
    [J]. EMBO JOURNAL, 1989, 8 (04) : 1067 - 1072
  • [6] THE COMPLETE SEQUENCE OF DYSTROPHIN PREDICTS A ROD-SHAPED CYTOSKELETAL PROTEIN
    KOENIG, M
    MONACO, AP
    KUNKEL, LM
    [J]. CELL, 1988, 53 (02) : 219 - 228
  • [7] AN AUTOSOMAL TRANSCRIPT IN SKELETAL-MUSCLE WITH HOMOLOGY TO DYSTROPHIN
    LOVE, DR
    HILL, DF
    DICKSON, G
    SPURR, NK
    BYTH, BC
    MARSDEN, RF
    WALSH, FS
    EDWARDS, YH
    DAVIES, KE
    [J]. NATURE, 1989, 339 (6219) : 55 - 58
  • [8] CRACE - A SIMPLE METHOD FOR IDENTIFICATION OF THE 5'-END OF MESSENGER-RNAS
    MARUYAMA, IN
    RAKOW, TL
    MARUYAMA, HI
    [J]. NUCLEIC ACIDS RESEARCH, 1995, 23 (18) : 3796 - 3797
  • [9] CHARACTERISTIC MESSENGER-RNA ABNORMALITY FOUND IN HALF THE PATIENTS WITH SEVERE HEMOPHILIA-A IS DUE TO LARGE DNA INVERSIONS
    NAYLOR, J
    BRINKE, A
    HASSOCK, S
    GREEN, PM
    GIANNELLI, F
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (11) : 1773 - 1778
  • [10] PHILIPPE C, GENOMICS, V27, P539