TY - JOUR
T1 - Definition of a 1.06-Mb region linked to neuroinflammation in humans, rats and mice
AU - Öckinger, Johan
AU - Serrano-Fernández, Pablo
AU - Möller, Steffen
AU - Ibrahim, Saleh M.
AU - Olsson, Tomas
AU - Jagodic, Maja
PY - 2006
Y1 - 2006
N2 - Unbiased identification of susceptibility genes might provide new insights into pathogenic mechanisms that govern complex inflammatory diseases such as multiple sclerosis. In this study we fine mapped Eae18a, a region on rat chromosome 10 that regulates experimental autoimmune encephalomyelitis (EAE), an animal model for multiple sclerosis. We utilized two independent approaches: (1) in silico mapping based on sequence similarity between human multiple sclerosis susceptibility regions and rodent EAE quantitative trait loci and (2) linkage mapping in an F10 (DA X PVG.AV1) rat advanced intercrossed line. The linkage mapping defines Eae18a to a 5-Mb region, which overlaps one intergenomic consensus region identified in silico. The combined approach confirms experimentally, for the first time, the accuracy of the in silico method. Moreover, the shared intersection between the results of both mapping techniques defines a 1.06-Mb region containing 13 candidate genes for the regulation of neuroinflammation in humans, rats, and mice.
AB - Unbiased identification of susceptibility genes might provide new insights into pathogenic mechanisms that govern complex inflammatory diseases such as multiple sclerosis. In this study we fine mapped Eae18a, a region on rat chromosome 10 that regulates experimental autoimmune encephalomyelitis (EAE), an animal model for multiple sclerosis. We utilized two independent approaches: (1) in silico mapping based on sequence similarity between human multiple sclerosis susceptibility regions and rodent EAE quantitative trait loci and (2) linkage mapping in an F10 (DA X PVG.AV1) rat advanced intercrossed line. The linkage mapping defines Eae18a to a 5-Mb region, which overlaps one intergenomic consensus region identified in silico. The combined approach confirms experimentally, for the first time, the accuracy of the in silico method. Moreover, the shared intersection between the results of both mapping techniques defines a 1.06-Mb region containing 13 candidate genes for the regulation of neuroinflammation in humans, rats, and mice.
UR - http://www.scopus.com/inward/record.url?scp=33746389790&partnerID=8YFLogxK
U2 - 10.1534/genetics.106.057406
DO - 10.1534/genetics.106.057406
M3 - Article
C2 - 16624898
AN - SCOPUS:33746389790
SN - 0016-6731
VL - 173
SP - 1539
EP - 1545
JO - Genetics
JF - Genetics
IS - 3
ER -