GENE-ENCODING PARATHYROID HORMONE-LIKE PEPTIDE - NUCLEOTIDE-SEQUENCE OF THE RAT GENE AND COMPARISON WITH THE HUMAN HOMOLOG

被引:67
作者
KARAPLIS, AC
YASUDA, T
HENDY, GN
GOLTZMAN, D
BANVILLE, D
机构
[1] ROYAL VICTORIA HOSP,MONTREAL H3A 1A1,QUEBEC,CANADA
[2] MCGILL UNIV,DEPT PHYSIOL & MED,CALCIUM RES LAB,MONTREAL H3A 1A1,QUEBEC,CANADA
[3] NATL RES COUNCIL CANADA,BIOTECHNOL RES INST,MOLEC GENET LAB,MONTREAL H4P 2R2,QUEBEC,CANADA
关键词
D O I
10.1210/mend-4-3-441
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The single-copy gene coding for rat PTH-like peptide was isolated from a rat liver genomic DNA library. The gene spans 12 kilobases and contains four exons. Exon I encodes the 5′-noncoding region, exon II encodes the prepro region, exon III encodes the mature peptide sequence up to amino acid 139 and exon IV encodes the carboxyl-terminal two amino acids, a stop codon, and the 3′-noncoding region. Splicing of these exons yields the 1.4 kilobase mRNA which is the predominant transcript observed in the hypercalcemic rat Leydig cell tumor and several normal rat tissues. The overall exon/intron organization of the rat parathyroid hormonelike peptide (PLP) gene is similar to that of the PTH gene and emphasizes the likelihood that PLP and PTH arose from a common ancestral gene. A comparison of the single promoter region of the rat with the second promoter of the human gene indicates conserved TATA and CAAT box homologies, GC box regions (SP-1 binding sites), putative AP-2 binding sites, and a vitamin D responsive element. When compared to the seven exon human PLP gene, which uses multiple promoters and encodes three peptide isoforms, the simpler organization of the rat gene predicts, in mammals, the predominant use of a single promoter and generation of a 141-amino acid peptide as the major molecular form. © 1990 by The Endocrine Society.
引用
收藏
页码:441 / 446
页数:6
相关论文
共 21 条
  • [1] THE PARATHYROID HORMONE-RELATED PROTEIN ASSOCIATED WITH MALIGNANCY IS SECRETED BY NEURO-ENDOCRINE TUMORS
    DEFTOS, LJ
    GAZDAR, AF
    IKEDA, K
    BROADUS, AE
    [J]. MOLECULAR ENDOCRINOLOGY, 1989, 3 (03) : 503 - 508
  • [2] CIRCULATING CONCENTRATIONS OF PARATHYROID HORMONE-LIKE PEPTIDE IN MALIGNANCY AND IN HYPERPARATHYROIDISM
    HENDERSON, JE
    SHUSTIK, C
    KREMER, R
    RABBANI, SA
    HENDY, GN
    GOLTZMAN, D
    [J]. JOURNAL OF BONE AND MINERAL RESEARCH, 1990, 5 (02) : 105 - 113
  • [3] IKEDA K, 1989, J BIOL CHEM, V264, P15743
  • [4] EXPRESSION OF MESSENGER RIBONUCLEIC-ACIDS ENCODING A PARATHYROID HORMONE-LIKE PEPTIDE IN NORMAL HUMAN AND ANIMAL-TISSUES WITH ABNORMAL EXPRESSION IN HUMAN PARATHYROID ADENOMAS
    IKEDA, K
    WEIR, EC
    MANGIN, M
    DANNIES, PS
    KINDER, B
    DEFTOS, LJ
    BROWN, EM
    BROADUS, AE
    [J]. MOLECULAR ENDOCRINOLOGY, 1988, 2 (12) : 1230 - 1236
  • [5] KEMER SA, 1989, P NATL ACAD SCI USA, V86, P1143
  • [6] KREMER R, 1989, J BONE MINER RES S1, V4, pA310
  • [7] STRUCTURE OF THE RAT OSTEOCALCIN GENE AND REGULATION OF VITAMIN-D-DEPENDENT EXPRESSION
    LIAN, J
    STEWART, C
    PUCHACZ, E
    MACKOWIAK, S
    SHALHOUB, V
    COLLART, D
    ZAMBETTI, G
    STEIN, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (04) : 1143 - 1147
  • [8] 2 DISTINCT TUMOR-DERIVED, PARATHYROID HORMONE-LIKE PEPTIDES RESULT FROM ALTERNATIVE RIBONUCLEIC-ACID SPLICING
    MANGIN, M
    IKEDA, K
    DREYER, BE
    MILSTONE, L
    BROADUS, AE
    [J]. MOLECULAR ENDOCRINOLOGY, 1988, 2 (11) : 1049 - 1055
  • [9] IDENTIFICATION OF A CDNA-ENCODING A PARATHYROID HORMONE-LIKE PEPTIDE FROM A HUMAN-TUMOR ASSOCIATED WITH HUMORAL HYPERCALCEMIA OF MALIGNANCY
    MANGIN, M
    WEBB, AC
    DREYER, BE
    POSILLICO, JT
    IKEDA, K
    WEIR, EC
    STEWART, AF
    BANDER, NH
    MILSTONE, L
    BARTON, DE
    FRANCKE, U
    BROADUS, AE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (02) : 597 - 601
  • [10] ISOLATION AND CHARACTERIZATION OF THE HUMAN PARATHYROID HORMONE-LIKE PEPTIDE GENE
    MANGIN, M
    IKEDA, K
    DREYER, BE
    BROADUS, AE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (07) : 2408 - 2412