Identification and characterization of two novel tetratricopeptide repeat-containing genes

被引:30
作者
Murthy, AE
Bernards, A
Church, D
Wasmuth, J
Gusella, JF
机构
[1] MASSACHUSETTS GEN HOSP,MOL NEUROGENET UNIT,CHARLESTOWN,MA 02129
[2] MASSACHUSETTS GEN HOSP,CTR CANC,CHARLESTOWN,MA 02129
[3] UNIV CALIF IRVINE,DEPT BIOL CHEM,IRVINE,CA 92717
[4] HARVARD UNIV,SCH MED,DEPT GENET,BOSTON,MA 02114
关键词
D O I
10.1089/dna.1996.15.727
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 tetratricopeptide repeat (TPR) is a degenerate, repeating amino acid motif of 34 residues that has been identified in a variety of proteins; however, no biochemical function has been established for it, In a two-hybrid screen for interaction with the GAP-related domain of neurofibromin, the product of the NF1 gene, we have identified two novel human genes encoding proteins with TPR motifs, The first, represented by cDNA tpr1, is located in chromosome 5q32-33.2, It is ubiquitously expressed as a 1.6-kb transcript that encodes three tandem TPR motifs, but is not related to any other known gene outside this domain, The second, defined by cDNA tpr2, maps to human chromosome 17q11.2-23. It is ubiquitously expressed as a 2.2-kb transcript encoding seven TPR units, Interestingly, a separate region of the tpr2 cDNA has striking similarity to the ''J region'' of the DnaJ family, The products of the tpr1 and tpr2 cDNAs interact preferentially with a truncated form of the NF1 GAP-related domain via their TPR regions, suggesting that they may be targeted to an abnormality of protein folding.
引用
收藏
页码:727 / 735
页数:9
相关论文
共 45 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   THE ITK RECEPTOR TYROSINE KINASE IS EXPRESSED IN PRE-B LYMPHOCYTES AND CEREBRAL NEURONS AND USES A NON-AUG TRANSLATIONAL INITIATOR [J].
BERNARDS, A ;
DELAMONTE, SM .
EMBO JOURNAL, 1990, 9 (07) :2279-2287
[3]   COMPLETE HUMAN NF1 CDNA SEQUENCE - 2 ALTERNATIVELY SPLICED MESSENGER-RNAS AND ABSENCE OF EXPRESSION IN A NEUROBLASTOMA LINE [J].
BERNARDS, A ;
HAASE, VH ;
MURTHY, AE ;
MENON, A ;
HANNIGAN, GE ;
GUSELLA, JF .
DNA AND CELL BIOLOGY, 1992, 11 (10) :727-734
[4]  
Blatch G. L., 1995, Proceedings of the American Association for Cancer Research Annual Meeting, V36, P68
[5]   MOLECULAR APPROACH TO ANALYZING THE HUMAN 5P DELETION SYNDROME, CRI-DU-CHAT [J].
CARLOCK, LR ;
WASMUTH, JJ .
SOMATIC CELL AND MOLECULAR GENETICS, 1985, 11 (03) :267-276
[6]   HUMAN HOMOLOGS OF THE BACTERIAL HEAT-SHOCK PROTEIN DNAJ ARE PREFERENTIALLY EXPRESSED IN NEURONS [J].
CHEETHAM, ME ;
BRION, JP ;
ANDERTON, BH .
BIOCHEMICAL JOURNAL, 1992, 284 :469-476
[7]  
CYR DM, 1992, J BIOL CHEM, V267, P20927
[8]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[9]   NUCLEAR TARGETING SEQUENCES - A CONSENSUS [J].
DINGWALL, C ;
LASKEY, RA .
TRENDS IN BIOCHEMICAL SCIENCES, 1991, 16 (12) :478-481
[10]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13