CD44 ISOFORM EXPRESSION MEDIATED BY ALTERNATIVE SPLICING - TISSUE-SPECIFIC REGULATION IN MICE

被引:40
作者
HIRANO, H [1 ]
SCREATON, GR [1 ]
BELL, MV [1 ]
JACKSON, DG [1 ]
BELL, JI [1 ]
HODES, RJ [1 ]
机构
[1] JOHN RADCLIFFE HOSP,INST MOLEC MED,MOLEC IMMUNOL GRP,OXFORD OX3 9DU,ENGLAND
关键词
ALTERNATIVE SPLICING; CD44; ISOFORM;
D O I
10.1093/intimm/6.1.49
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD44 is a widely distributed cell surface glycoprotein which shows heterogeneity in molecular expression as a result of post-translational modification as well as alternative splicing of CD44 mRNA. Functional studies have indicated that CD44 plays a role as an adhesion molecule and that different CD44-expressing cells differ in their capacities for CD44-dependent ligand binding. These observations have raised the possibility that structural modifications of CD44, including those resulting from alternatively spliced mRNA isoforms, are involved in the functional heterogeneity of CD44. To assess the expression of CD44 isoforms in the mouse, we examined CD44 cDNA by reverse transcription polymerase chain reaction (RT-PCR). Southern blotting of PCR products with a CD44 cDNA probe or with internal oligonucleotides revealed the expression in mouse tumor cell lines and normal tissues of multiple CD44 mRNA products which are larger than that observed in the absence of variable exon expression. Interestingly, different mouse tissues, including lymphoid cells, showed unique patterns of alternative CD44 mRNA in Southern blotting analysis. The use of exon-specific primers allowed detection of multiple alternatively spliced mRNA species involving expression of at least seven variable exons. Cloning and sequencing of these PCR products revealed sequence identity with recently identified genomic CD44 sequences and confirmed that the PCR products correspond to mature mRNA expressing alternatively spliced CD44 exons. Taken together, these findings demonstrate that the mouse expresses multiple variably spliced CD44 isoforms and that expression is regulated in a tissue- and cell-type specific manner.
引用
收藏
页码:49 / 59
页数:11
相关论文
共 47 条
[11]  
GOLDSTEIN LA, 1990, IMMUNOGENETICS, V32, P389
[12]   A HUMAN-LYMPHOCYTE HOMING RECEPTOR, THE HERMES ANTIGEN, IS RELATED TO CARTILAGE PROTEOGLYCAN CORE AND LINK PROTEINS [J].
GOLDSTEIN, LA ;
ZHOU, DFH ;
PICKER, LJ ;
MINTY, CN ;
BARGATZE, RF ;
DING, JF ;
BUTCHER, EC .
CELL, 1989, 56 (06) :1063-1072
[13]   A NEW VARIANT OF GLYCOPROTEIN CD44 CONFERS METASTATIC POTENTIAL TO RAT CARCINOMA-CELLS [J].
GUNTHERT, U ;
HOFMANN, M ;
RUDY, W ;
REBER, S ;
ZOLLER, M ;
HAUSSMANN, I ;
MATZKU, S ;
WENZEL, A ;
PONTA, H ;
HERRLICH, P .
CELL, 1991, 65 (01) :13-24
[14]  
HATHCOCK KS, 1992, J IMMUNOL, V149, P2286
[15]   CD44 - A MOLECULE INVOLVED IN LEUKOCYTE ADHERENCE AND T-CELL ACTIVATION [J].
HAYNES, BF ;
TELEN, MJ ;
HALE, LP ;
DENNING, SM .
IMMUNOLOGY TODAY, 1989, 10 (12) :423-428
[16]   MOLECULAR ISOFORMS OF MURINE CD44 AND EVIDENCE THAT THE MEMBRANE PROXIMAL DOMAIN IS NOT CRITICAL FOR HYALURONATE RECOGNITION [J].
HE, Q ;
LESLEY, J ;
HYMAN, R ;
ISHIHARA, K ;
KINCADE, PW .
JOURNAL OF CELL BIOLOGY, 1992, 119 (06) :1711-1719
[17]  
HECHT TT, 1983, J IMMUNOL, V131, P1049
[18]   A HUMAN HOMOLOG OF THE RAT METASTASIS-ASSOCIATED VARIANT OF CD44 IS EXPRESSED IN COLORECTAL CARCINOMAS AND ADENOMATOUS POLYPS [J].
HEIDER, KH ;
HOFMANN, M ;
HORS, E ;
VANDENBERG, F ;
PONTA, H ;
HERRLICH, P ;
PALS, ST .
JOURNAL OF CELL BIOLOGY, 1993, 120 (01) :227-233
[19]  
HOFMANN M, 1991, CANCER RES, V51, P5292
[20]  
HUET S, 1989, J IMMUNOL, V143, P798