THE STRUCTURE AND EVOLUTION OF THE HUMAN SALIVARY PROLINE-RICH PROTEIN GENE FAMILY

被引:34
作者
KIM, HS
LYONS, KM
SAITOH, E
AZEN, EA
SMITHIES, O
MAEDA, N
机构
[1] VANDERBILT UNIV,MED CTR,SCH MED,DEPT CELL BIOL,NASHVILLE,TN 37232
[2] NIPPON DENT UNIV,DEPT ORAL BIOCHEM,NIIGATA 951,JAPAN
[3] UNIV WISCONSIN,DEPT MED,MADISON,WI 53706
[4] UNIV WISCONSIN,DEPT MED GENET,MADISON,WI 53706
关键词
D O I
10.1007/BF00364656
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 present the nucleotide sequences of four members of the six-member human salivary proline-rich protein (PRP) gene family. The four genes are PRB1 and PRB2, which encode basic PRPs, and PRB3 and PRB4, which encode glycosylated PRPs. Each PRB gene is approximately 4.0 kb in length and contains four exons, the third of which is entirely composed of 63-bp tandem repeats and encodes the proline-rich portion of the protein products. Exon 3 contains different numbers of tandem repeats in the different PRB genes. Variation in the numbers of these repeats is also responsible for length variations in different alleles of the PRB genes. We have determined a probable evolutionary history of the human PRP gene family by comparing the nucleotide sequences of the six PRP genes. The present-day six PRP loci probably evolved from a single ancestral gene by four sequential gene duplications, leading to six genes that fall into three subsets, each consisting of two genes. During this evolutionary process, multiple rearrangements and gene conversion occurred mainly in the region from the 3' end of IVS2 and the 3' end of exon 3.
引用
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页码:3 / 14
页数:12
相关论文
共 38 条
  • [1] CLONES FROM THE HUMAN-GENE COMPLEX CODING FOR SALIVARY PROLINE-RICH PROTEINS
    AZEN, E
    LYONS, KM
    MCGONIGAL, T
    BARRETT, NL
    CLEMENTS, LS
    MAEDA, N
    VANIN, EF
    CARLSON, DM
    SMITHIES, O
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (17): : 5561 - 5565
  • [2] AZEN EA, 1987, AM J HUM GENET, V41, P1035
  • [3] MESSENGER-RNAS FOR PRPS, STATHERIN, AND HISTATINS IN VONEBNER GLAND TISSUES
    AZEN, EA
    HELLEKANT, G
    SABATINI, LM
    WARNER, TF
    [J]. JOURNAL OF DENTAL RESEARCH, 1990, 69 (11) : 1724 - 1730
  • [4] BENNICK A, 1982, MOL CELL BIOCHEM, V45, P83
  • [5] THE ROLE OF HUMAN SALIVARY ACIDIC PROLINE-RICH PROTEINS IN THE FORMATION OF ACQUIRED DENTAL PELLICLE INVIVO AND THEIR FATE AFTER ADSORPTION TO THE HUMAN-ENAMEL SURFACE
    BENNICK, A
    CHAU, G
    GOODLIN, R
    ABRAMS, S
    TUSTIAN, D
    MADAPALLIMATTAM, G
    [J]. ARCHIVES OF ORAL BIOLOGY, 1983, 28 (01) : 19 - 27
  • [6] ISOLATION AND NUCLEOTIDE-SEQUENCE ANALYSIS OF THE BETA-TYPE GLOBIN PSEUDOGENE FROM HUMAN, GORILLA AND CHIMPANZEE
    CHANG, LYE
    SLIGHTOM, JL
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1984, 180 (04) : 767 - 783
  • [7] THE HUMAN GROWTH-HORMONE LOCUS - NUCLEOTIDE-SEQUENCE, BIOLOGY, AND EVOLUTION
    CHEN, EY
    LIAO, YC
    SMITH, DH
    BARRERASALDANA, HA
    GELINAS, RE
    SEEBURG, PH
    [J]. GENOMICS, 1989, 4 (04) : 479 - 497
  • [8] A RAPID SINGLE-STRANDED CLONING STRATEGY FOR PRODUCING A SEQUENTIAL SERIES OF OVERLAPPING CLONES FOR USE IN DNA SEQUENCING - APPLICATION TO SEQUENCING THE CORN MITOCHONDRIAL 18-S RDNA
    DALE, RMK
    MCCLURE, BA
    HOUCHINS, JP
    [J]. PLASMID, 1985, 13 (01) : 31 - 40
  • [9] 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
  • [10] THE STRUCTURE AND EVOLUTION OF THE HUMAN BETA-GLOBIN GENE FAMILY
    EFSTRATIADIS, A
    POSAKONY, JW
    MANIATIS, T
    LAWN, RM
    OCONNELL, C
    SPRITZ, RA
    DERIEL, JK
    FORGET, BG
    WEISSMAN, SM
    SLIGHTOM, JL
    BLECHL, AE
    SMITHIES, O
    BARALLE, FE
    SHOULDERS, CC
    PROUDFOOT, NJ
    [J]. CELL, 1980, 21 (03) : 653 - 668