The human cysteine-rich secretory protein (CRISP) family primary structure and tissue distribution of CRISP-1, CRISP-2 and CRISP-3

被引:188
作者
Kratzschmar, J
Haendler, B
Eberspaecher, U
Roosterman, D
Donner, P
Schleuning, WD
机构
[1] Research Laboratories of Schering AG, Berlin
[2] Inst. of Cell. and Molecular Biology, Schering AG
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1996年 / 236卷 / 03期
关键词
human cDNA; cysteine-rich; secretory; epididymis; salivary gland;
D O I
10.1111/j.1432-1033.1996.t01-1-00827.x
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
We report the isolation and characterisation of cDNAs encoding three different, human members of the cysteine-rich secretory protein (CRISP) family. The novel CRISP-1 exists in five cDNA subtypes differing by the presence or absence of a stretch coding for a C-terminal cysteine-rich domain so far found in all members of the family, and by the length of their 3'-untranslated region. CRISP-2 cDNA corresponds to the previously described TPX1 form, with so far unreported 5'-untranslated sequence heterogeneities while CRISP-3 cDNA codes for a new, unique protein. Northern blot analysis of various human organs indicates that CRISP-1 transcripts are epididymis-specific whereas CRISP-UTPX1 transcripts are detected mainly in the testis and also in the epididymis. CRISP-3 transcripts are more widely distributed and found predominantly in the salivary gland, pancreas and prostate, and in less abundance in the epididymis, ovary, thymus and colon. A protein reacting with an anti-mouse CRISP-1 antibody was isolated from human epididymal extracts and N-terminal sequencing revealed that it corresponded to the CRISP-1 cDNA we have isolated. In contrast to findings on its rat counterpart epididymal protein DE/acidic epididymal glycoprotein (AEG), no significant association of CRISP-1 with human spermatozoa was observed.
引用
收藏
页码:827 / 836
页数:10
相关论文
共 44 条
  • [1] INCREASED TOLERANCE TO 2 OOMYCETE PATHOGENS IN TRANSGENIC TOBACCO EXPRESSING PATHOGENESIS-RELATED PROTEIN-1A
    ALEXANDER, D
    GOODMAN, RM
    GUTRELLA, M
    GLASCOCK, C
    WEYMANN, K
    FRIEDRICH, L
    MADDOX, D
    AHLGOY, P
    LUNTZ, T
    WARD, E
    RYALS, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (15) : 7327 - 7331
  • [2] ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
  • [4] MOLECULAR-CLONING OF THE CDNA FOR ANDROGEN-DEPENDENT SPERM-COATING GLYCOPROTEINS SECRETED BY THE RAT EPIDIDYMIS
    BROOKS, DE
    MEANS, AR
    WRIGHT, EJ
    SINGH, SP
    TIVER, KK
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 161 (01): : 13 - 18
  • [5] BROOKS DE, 1983, J REPROD FERTIL, V69, P651, DOI 10.1530/jrf.0.0690651
  • [6] BURNETTE WN, 1981, ANAL BIOCHEM, V112, P195, DOI 10.1016/0003-2697(81)90281-5
  • [7] ANDROGEN-CONTROLLED SPECIFIC PROTEINS IN RAT EPIDIDYMIS
    CAMEO, MS
    GLAQUIER, JA
    [J]. JOURNAL OF ENDOCRINOLOGY, 1976, 69 (01) : 47 - 55
  • [8] MOLECULAR-CLONING OF COMPLEMENTARY DEOXYRIBONUCLEIC-ACID FOR AN ANDROGEN-REGULATED EPIDIDYMAL PROTEIN - SEQUENCE HOMOLOGY WITH METALLOPROTEINS
    CHAREST, NJ
    JOSEPH, DR
    WILSON, EM
    FRENCH, FS
    [J]. MOLECULAR ENDOCRINOLOGY, 1988, 2 (10) : 999 - 1004
  • [9] SIGNAL PEPTIDASES IN PROKARYOTES AND EUKARYOTES - A NEW PROTEASE FAMILY
    DALBEY, RE
    VONHEIJNE, G
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (11) : 474 - 478
  • [10] A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX
    DEVEREUX, J
    HAEBERLI, P
    SMITHIES, O
    [J]. NUCLEIC ACIDS RESEARCH, 1984, 12 (01) : 387 - 395