Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded rat

被引:232
作者
Brown, DM
Provoost, AP
Daly, MJ
Lander, ES
Jacob, HJ
机构
[1] HARVARD UNIV, SCH MED, MASSACHUSETTS GEN HOSP, CARDIOVASC RES CTR, BOSTON, MA 02129 USA
[2] ERASMUS UNIV ROTTERDAM, DEPT PEDIAT SURG, ROTTERDAM, NETHERLANDS
[3] WHITEHEAD INST BIOMED RES, MIT, CTR GENOME RES, CAMBRIDGE, MA 02142 USA
[4] MIT, DEPT BIOL, CAMBRIDGE, MA 02139 USA
关键词
D O I
10.1038/ng0196-44
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Hypertension, diabetes and hyperlipidemia are risk factors for life-threatening complications such as end-stage renal disease, coronary artery disease and stroke. Why some patients develop complications is unclear, but only susceptibility genes may be involved. To test this notion, we studied crosses involving the fawn-hooded rat, an animal model of hypertension that develops chronic renal failure. Here, we report the localization of two genes, Rf-1 and Rf-2, responsible for about half of the genetic variation in key indices of renal impairment. In addition, we localize a gene, Bpfh-1, responsible for about 26% of the genetic variation in blood pressure. Rf-1 strongly affects the risk of renal impairment, but has no significant effect on blood pressure. Our results show that susceptibility to a complication of hypertension is under at feast partially independent genetic control from susceptibility to hypertension itself.
引用
收藏
页码:44 / 51
页数:8
相关论文
共 56 条
  • [1] BAKER HJ, 1979, LABORATORY RAT BIOL, V1, P88
  • [2] POTENTIATION OF UREMIC BLEEDING BY HEREDITARY STORAGE POOL DISEASE
    BERTY, RM
    ZEIGLER, ZR
    BRUNS, FJ
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1992, 19 (04) : 326 - 330
  • [3] EPIDEMIOLOGIC ANALYSIS OF EXISTING DATA TO INVESTIGATE HYPERTENSIVE RENAL-DISEASE - AN EXAMPLE FROM THE MARYLAND-END-STAGE-RENAL-DISEASE-REGISTRY
    BRANCATI, FL
    WHELTON, PK
    WHITTLE, JC
    KLAG, MJ
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 1993, 21 (04) : 15 - 24
  • [4] BRANDIS A, 1986, LAB INVEST, V55, P234
  • [5] PROGRESSION OF RENAL-INSUFFICIENCY - ROLE OF BLOOD-PRESSURE
    BRAZY, PC
    STEAD, WW
    FITZWILLIAM, JF
    [J]. KIDNEY INTERNATIONAL, 1989, 35 (02) : 670 - 674
  • [6] BRENNER BM, 1982, NEW ENGL J MED, V307, P652, DOI 10.1056/NEJM198209093071104
  • [7] CHUNG O, 1993, RAT MODELS CHRONIC R, P357
  • [8] LINKAGE OF 11-BETA-HYDROXYLASE MUTATIONS WITH ALTERED STEROID-BIOSYNTHESIS AND BLOOD-PRESSURE IN THE DAHL RAT
    CICILA, GT
    RAPP, JP
    WANG, JM
    STLEZIN, E
    NG, SC
    KURTZ, TW
    [J]. NATURE GENETICS, 1993, 3 (04) : 346 - 353
  • [9] GENETIC IDENTIFICATION OF MOM-1, A MAJOR MODIFIER LOCUS AFFECTING MIN-INDUCED INTESTINAL NEOPLASIA IN THE MOUSE
    DIETRICH, WF
    LANDER, ES
    SMITH, JS
    MOSER, AR
    GOULD, KA
    LUONGO, C
    BORENSTEIN, N
    DOVE, W
    [J]. CELL, 1993, 75 (04) : 631 - 639
  • [10] GENETIC-DETERMINANTS OF DIASTOLIC AND PULSE PRESSURE MAP TO DIFFERENT LOCI IN LYON HYPERTENSIVE RATS
    DUBAY, C
    VINCENT, M
    SAMANI, NJ
    HILBERT, P
    KAISER, MA
    BERESSI, JP
    KOTELEVTSEV, Y
    BECKMANN, JS
    SOUBRIER, F
    SASSARD, J
    LATHROP, GM
    [J]. NATURE GENETICS, 1993, 3 (04) : 354 - 357