HEREDITARY HYPERTENSION CAUSED BY CHIMERIC GENE DUPLICATIONS AND ECTOPIC EXPRESSION OF ALDOSTERONE SYNTHASE

被引:261
作者
LIFTON, RP
DLUHY, RG
POWERS, M
RICH, GM
GUTKIN, M
FALLO, F
GILL, JR
FELD, L
GANGULY, A
LAIDLAW, JC
MURNAGHAN, DJ
KAUFMAN, C
STOCKIGT, JR
ULICK, S
LALOUEL, JM
机构
[1] UNIV UTAH,DEPT HUMAN GENET,SALT LAKE CITY,UT 84112
[2] BRIGHAM & WOMENS HOSP,DIV ENDOCRINE HYPERTENS,BOSTON,MA 02115
[3] HYPERTENS RENAL GRP,LIVINGSTON,NJ 07039
[4] UNIV PADUA,INST SEMEIOT MED,I-35100 PADUA,ITALY
[5] NHLBI,BETHESDA,MD 20892
[6] CHILDRENS HOSP,DIV NEPHROL,BUFFALO,NY 14222
[7] UNIV S FLORIDA,COLL MED,DEPT MED,TAMPA,FL 33620
[8] CANADIAN CANC SOC,TORONTO M4V 3B1,ONTARIO,CANADA
[9] REG HOSP CORK,DEPT MED,CORK,IRELAND
[10] UNIV OKLAHOMA,HLTH SCI CTR,NEPHROL SECT,OKLAHOMA CITY,OK 73112
[11] ALFRED HOSP,EWEN DOWNIE METAB UNIT,MELBOURNE,VIC 3181,AUSTRALIA
[12] VET AFFAIRS HOSP,BRONX,NY 10468
关键词
D O I
10.1038/ng0992-66
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Patients with glucocorticoid-remediable aldosteronism (GRA) from 12 kindreds possess chimaeric gene duplications arising from unequal crossing-over, fusing regulatory sequences of steroid 11-beta-hydroxylase to coding sequences of aldosterone synthase. These chimaeric genes are specific for GRA and explain the biochemistry, physiology and genetics of this form of hypertension. Sites of crossing over range from intron 2 to intron 4. Most mutations have arisen independently from either sister or non-sister chromatid exchange between these genes, which are only 45 kilobases apart. The possibility of a susceptibility allele for GRA of Irish origin is suggested. These findings indicate the utility of a direct genetic test for this disorder.
引用
收藏
页码:66 / 74
页数:9
相关论文
共 32 条
  • [1] POLYMORPHIC DNA REGION ADJACENT TO THE 5'-END OF THE HUMAN INSULIN GENE
    BELL, GI
    KARAM, JH
    RUTTER, WJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (09): : 5759 - 5763
  • [2] CHU MD, 1982, J BIOL CHEM, V257, P2218
  • [3] CLONING OF CDNA-ENCODING STEROID 11-BETA-HYDROXYLASE (P450C11)
    CHUA, SC
    SZABO, P
    VITEK, A
    GRZESCHIK, KH
    JOHN, M
    WHITE, PC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (20) : 7193 - 7197
  • [4] FALLO F, CLIN ENDOCRINOL, V22, P777
  • [5] A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY
    FEINBERG, AP
    VOGELSTEIN, B
    [J]. ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) : 6 - 13
  • [6] FRACTIONATION OF LARGE MAMMALIAN DNA RESTRICTION FRAGMENTS USING VERTICAL PULSED-FIELD GRADIENT GEL-ELECTROPHORESIS
    GARDINER, K
    LAAS, W
    PATTERSON, D
    [J]. SOMATIC CELL AND MOLECULAR GENETICS, 1986, 12 (02) : 185 - 195
  • [7] KINDRED WITH FAMILIAL GLUCOCORTICOID-SUPPRESSIBLE ALDOSTERONISM
    GIEBINK, GS
    GOTLIN, RW
    BIGLIERI, EG
    KATZ, FH
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1973, 36 (04) : 715 - 723
  • [8] ANALYSIS OF CYTOKINE MESSENGER-RNA AND DNA - DETECTION AND QUANTITATION BY COMPETITIVE POLYMERASE CHAIN-REACTION
    GILLILAND, G
    PERRIN, S
    BLANCHARD, K
    BUNN, HF
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (07) : 2725 - 2729
  • [9] ELEVATED URINARY-EXCRETION OF 18-OXOCORTISOL IN GLUCOCORTICOID-SUPPRESSIBLE ALDOSTERONISM
    GOMEZSANCHEZ, CE
    MONTGOMERY, M
    GANGULY, A
    HOLLAND, OB
    GOMEZSANCHEZ, EP
    GRIM, CE
    WEINBERGER, MH
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1984, 59 (05) : 1022 - 1024
  • [10] GRIM CE, 1980, PEDIATRICS, V65, P597