Human testis specifically expresses a homologue of the rodent T lymphocytes RT6 mRNA

被引:24
作者
Levy, I
Wu, YQ
Roeckel, N
Bulle, F
Pawlak, A
Siegrist, S
Mattei, MG
Guellaen, G
机构
[1] HOP HENRI MONDOR,U INSERM 99,F-94010 CRETEIL,FRANCE
[2] HOP ENFANTS LA TIMONE,U INSERM 406,F-13385 MARSEILLE,FRANCE
关键词
human testis; mono ADP-ribosyl transferase; RT6; chromosome; 4; diabetes mellitus;
D O I
10.1016/0014-5793(96)00183-4
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
A human homologue of the rodent T cell mono ADP-ribosyl transferase RT6 mRMA was identified by a systematic analysis of human testis transcripts. This messenger encodes for a precursor protein of 367 aa (MW: 41.5 kDa) which exhibits a peptide signal, consensus domains for mono ADP-ribosyl transferase and a C-terminal part characteristic of glycophosphatidyl inositol anchored protein. This mRNA, transcribed from a gene localized in 4q13-q21, is not expressed in white blood cells but is specific for human testis in which it is likely to correspond to a new ADP-ribosyl transferase.
引用
收藏
页码:276 / 280
页数:5
相关论文
共 28 条
[1]   PREVENTION OF DIABETES IN BB/WOR RAT BY SINGLE TRANSFUSION OF SPLEEN-CELLS - PARAMETERS THAT AFFECT DEGREE OF PROTECTION [J].
BURSTEIN, D ;
MORDES, JP ;
GREINER, DL ;
STEIN, D ;
NAKAMURA, N ;
HANDLER, ES ;
ROSSINI, AA .
DIABETES, 1989, 38 (01) :24-30
[2]   AN RT6A GENE IS TRANSCRIBED AND TRANSLATED IN LYMPHOPENIC DIABETES-PRONE BB RATS [J].
CRISA, L ;
SARKAR, P ;
WAITE, DJ ;
FRIEDRICH, FH ;
KOCHNOLTE ;
RAJAN, TV ;
MORDES, JP ;
HANDLER, ES ;
THIELE, HG ;
ROSSINI, AA ;
GREINER, DL .
DIABETES, 1993, 42 (05) :688-695
[3]   BIOCHEMICAL-STUDIES OF RT6 ALLOANTIGENS IN BB/WOR AND NORMAL RATS - EVIDENCE FOR INTACT UNEXPRESSED RT6A STRUCTURAL GENE IN DIABETES-PRONE BB RATS [J].
CRISA, L ;
GREINER, DL ;
MORDES, JP ;
MACDONALD, RG ;
HANDLER, ES ;
CZECH, MP ;
ROSSINI, AA .
DIABETES, 1990, 39 (10) :1279-1288
[4]   DIABETES-PRONE BB RATS EXPRESS THE RT6 ALLOANTIGEN ON INTESTINAL INTRAEPITHELIAL LYMPHOCYTES [J].
FANGMANN, J ;
SCHWINZER, R ;
HEDRICH, HJ ;
KLOTING, I ;
WONIGEIT, K .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1991, 21 (09) :2011-2015
[5]  
FERGUSON MAJ, 1988, ANNU REV BIOCHEM, V57, P285
[6]   EXPRESSED SEQUENCE TAGS IDENTIFY A HUMAN ISOLOG OF THE SUI1 TRANSLATION INITIATION-FACTOR [J].
FIELDS, C ;
ADAMS, MD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 198 (01) :288-291
[7]   EVIDENCE THAT THE T-CELL REPERTOIRE OF NORMAL RATS CONTAINS CELLS WITH THE POTENTIAL TO CAUSE DIABETES - CHARACTERIZATION OF THE CD4+ T-CELL SUBSET THAT INHIBITS THIS AUTOIMMUNE POTENTIAL [J].
FOWELL, D ;
MASON, D .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (03) :627-636
[8]  
GREINER DL, 1986, J IMMUNOL, V136, P148
[9]   BOTH ALLELIC FORMS OF THE RAT T-CELL DIFFERENTIATION MARKER RT6 DISPLAY NICOTINAMIDE ADENINE-DINUCLEOTIDE (NAD)-GLYCOHYDROLASE ACTIVITY, YET ONLY RT6.2 IS CAPABLE OF AUTOMODIFICATION UPON INCUBATION WITH NAD [J].
HAAG, F ;
ANDRESEN, V ;
KARSTEN, S ;
KOCHNOLTE, F ;
THIELE, HG .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1995, 25 (08) :2355-2361
[10]   NUCLEOTIDE AND DEDUCED AMINO-ACID-SEQUENCE OF THE RAT T-CELL ALLOANTIGEN RT6.1 [J].
HAAG, F ;
KOCH, F ;
THIELE, HG .
NUCLEIC ACIDS RESEARCH, 1990, 18 (04) :1047-1047