Quantitative trait loci for peripheral blood cell counts: a study in baboons

被引:7
作者
Bertin, Angeline [1 ]
Mahaney, Michael C.
Cox, Laura A.
Rogers, Jeffrey
VandeBerg, John L.
Brugnara, Carlo
Platt, Orah S.
机构
[1] SW Fdn Biomed Res, Dept Genet, San Antonio, TX 78245 USA
[2] SW Fdn Biomed Res, SW Natl Primate Res Ctr, San Antonio, TX 78245 USA
[3] Harvard Univ, Sch Med, Childrens Hosp Boston, Boston, MA 02115 USA
关键词
D O I
10.1007/s00335-007-9022-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Increasingly, baseline peripheral blood cell counts are implicated as risk factors for common complex diseases. While genetic influences on these hematologic parameters are firmly established, the genetic architecture of the blood counts is still poorly understood. In this article we used data from 582 healthy pedigreed baboons and variance components methods to localize quantitative trait loci (QTLs) influencing complete blood count variables. Besides performing genome-wide linkage scans for each trait individually, we conducted bivariate linkage analyses for all pairwise trait combinations to also identify pleiotropic QTLs influencing several blood counts. While significant and suggestive QTLs were localized throughout the genome (LOD range: 1.5-3.5), chromosomal regions associated with the expression of various hematologic parameters stand out. In particular, our results provide significant and consistent evidence for a QTL on the orthologous human chromosome 1p that is shared by several blood counts, mainly erythrocyte parameters. In addition, multiple suggestive evidence of linkage was detected on the orthologous human chromosomes 10 (near the q-terminus) and 19 (centromeric section). Future studies should help identify the genes responsible for these QTL and elucidate their role on baseline variation in hematologic indicators of health and disease.
引用
收藏
页码:361 / 372
页数:12
相关论文
共 51 条
[1]   Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure [J].
Allison, DB ;
Neale, MC ;
Zannolli, R ;
Schork, NJ ;
Amos, CI ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (02) :531-544
[2]  
Almasy L, 1997, GENET EPIDEMIOL, V14, P953, DOI 10.1002/(SICI)1098-2272(1997)14:6<953::AID-GEPI65>3.0.CO
[3]  
2-K
[4]   Multipoint quantitative-trait linkage analysis in general pedigrees [J].
Almasy, L ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1198-1211
[5]   Comparison of multivariate tests for genetic linkage [J].
Amos, CI ;
de Andrade, M ;
Zhu, DK .
HUMAN HEREDITY, 2001, 51 (03) :133-144
[6]  
AMOS CI, 1994, AM J HUM GENET, V54, P535
[7]  
[Anonymous], 1992, LIKELIHOOD, DOI DOI 10.56021/9780801844454
[8]   Ethnic and sex differences in the total and differential white cell count and platelet count [J].
Bain, BJ .
JOURNAL OF CLINICAL PATHOLOGY, 1996, 49 (08) :664-666
[9]   Association of mean platelet volume with risk of stroke among 3134 individuals with history of cerebrovascular disease [J].
Bath, P ;
Algert, C ;
Chapman, N ;
Neal, B .
STROKE, 2004, 35 (03) :622-626
[10]   Variance component methods for detecting complex trait loci [J].
Blangero, J ;
Williams, JT ;
Almasy, L .
GENETIC DISSECTION OF COMPLEX TRAITS, 2001, 42 :151-181