Chromosomal mapping of quantitative trait loci contributing to stroke in a rat model of complex human disease

被引:220
作者
Rubattu, S
Volpe, M
Kreutz, R
Ganten, U
Ganten, D
Lindpaintner, K
机构
[1] BRIGHAM & WOMENS HOSP, DIV CARDIOVASC, BOSTON, MA 02115 USA
[2] UNIV NAPLES FEDERICO II, DEPT INTERNAL MED, I-80131 NAPLES, ITALY
[3] IST NEUROL MEDITERRANEO NEUROMED, I-86067 POZZILLI, ITALY
[4] UNIV ROMA LA SAPIENZA, DEPT EXPT MED & PATHOL, I-00100 ROME, ITALY
[5] MAX DELBRUCK CTR MOLEC MED, D-13122 BERLIN, GERMANY
关键词
D O I
10.1038/ng0896-429
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Stroke is a complex disorder with a poorly understood multifactorial and polygenic aetiology. We used the stroke-prone spontaneously hypertensive rat (SHRSP) as a model organism, mated it with the stroke-resistant spontaneously hypertensive rat (SHR) and performed a genome-wide screen in the resultant F2 cohort where latency until stroke, but not hypertension (a major confounder) segregated. We identified three major quantitative trait loci, STR1-3, with lod scores of 7.4, 4.7 and 3.0, respectively, that account for 28% of the overall phenotypic variance. STR2 colocalizes with the genes encoding atrial and brain natriuretic factor, peptides with important vasoactive properties. Our results demonstrate the existence of primary, blood pressure-independent genetic factors predisposing to a complex form of stroke.
引用
收藏
页码:429 / 434
页数:6
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