Chromosomal organization of candidate genes involved in cholesterol gallstone formation: A murine gallstone map

被引:179
作者
Lammert, F
Carey, MC
Paigen, B
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Dept Med,Div Gastroenterol, Boston, MA 02115 USA
[2] Harvard Univ, Ctr Digest Dis, Boston, MA 02115 USA
[3] Jackson Lab, Bar Harbor, ME 04609 USA
[4] Rhein Westfal TH Aachen Klinikum, Dept Med 3, Aachen, Germany
关键词
D O I
10.1053/gast.2001.20878
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Epidemiologic and family studies indicate that cholesterol gallstone formation is in part genetically determined. The major contribution to our current understanding of gallstone genes derives from animal studies, particularly cross-breeding experiments in inbred mouse strains that differ in genetic susceptibility to cholesterol gallstone formation (quantitative trait loci mapping). In this review we summarize how the combined use of genomic strategies and phenotypic studies in inbred mice has proven to be a powerful means of dissecting the complex pathophysiology of this common disease. We present a "gallstone map" for the mouse, consisting of all genetic loci that have been identified to confer gallstone susceptibility as well as putative candidate genes. Translation of the genetic loci and genes between mouse and human predicts chromosomal regions in the human genome that are likely to harbor gallstone genes. Both the number and the precise understanding of gallstone genes are expected to further increase with rapid progress of the genome projects, and multiple new targets for early diagnosis and prevention of gallstone disease should become possible.
引用
收藏
页码:221 / 238
页数:18
相关论文
共 167 条
[1]
Identification of scavenger receptor SR-BI as a high density lipoprotein receptor [J].
Acton, S ;
Rigotti, A ;
Landschulz, KT ;
Xu, SZ ;
Hobbs, HH ;
Krieger, M .
SCIENCE, 1996, 271 (5248) :518-520
[2]
Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats [J].
Aitman, TJ ;
Glazier, AM ;
Wallace, CA ;
Cooper, LD ;
Norsworthy, PJ ;
Wahid, FN ;
Al-Majali, KM ;
Trembling, PM ;
Mann, CJ ;
Shoulders, CC ;
Graf, D ;
St Lezin, E ;
Kurtz, TW ;
Kren, V ;
Pravenec, M ;
Ibrahimi, A ;
Abumrad, NA ;
Stanton, LW ;
Scott, J .
NATURE GENETICS, 1999, 21 (01) :76-83
[3]
Transgenic mice expressing human phospholipid transfer protein have increased HDL non-HDL cholesterol ratio [J].
Albers, JJ ;
Tu, AY ;
Paigen, B ;
Chen, H ;
Cheung, MC ;
Marcovina, SM .
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 1996, 26 (04) :262-267
[4]
DIFFERENT SUSCEPTIBILITIES TO THE FORMATION OF CHOLESTEROL GALLSTONES IN MICE [J].
ALEXANDER, M ;
PORTMAN, OW .
HEPATOLOGY, 1987, 7 (02) :257-265
[5]
Pathogenesis of cholesterol gallstones: A parsimonious hypothesis [J].
Apstein, MD ;
Carey, MC .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1996, 26 (05) :343-352
[6]
Bahar R, 1997, GASTROENTEROLOGY, V112, pA1219
[7]
Bile acid transport [J].
Bahar, RJ ;
Stolz, A .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 1999, 28 (01) :27-+
[8]
BANASZAK L, 1994, ADV PROTEIN CHEM, V45, P89
[9]
Apolipoprotein E polymorphism and gallstones [J].
Bertomeu, A ;
Ros, E ;
Zambon, D ;
Vela, M ;
PerezAyuso, RM ;
Targarona, E ;
Trias, M ;
Sanllehy, C ;
Casals, E ;
Ribo, JM .
GASTROENTEROLOGY, 1996, 111 (06) :1603-1610
[10]
ILEAL LIPID-BINDING PROTEIN (ILLBP) GENE MAPS TO MOUSE CHROMOSOME-11 [J].
BIRKENMEIER, EH ;
ROWE, LB ;
CROSSMAN, MW ;
GORDON, JI .
MAMMALIAN GENOME, 1994, 5 (12) :805-806