Two ENU-induced mutations in Rasgrf1 and early mouse growth retardation

被引:26
作者
Clapcott, SJ
Peters, J
Orban, PC
Brambilla, R
Graham, CF
机构
[1] Dept Zool, Oxford OX1 3PS, England
[2] MRC, Mammalian Genet Unit, Didcot OX11 0RD, Oxon, England
[3] Ist Sci San Raffaele, Dept Biol & Technol Res, I-20132 Milan, Lombardy, Italy
关键词
D O I
10.1007/s00335-002-2258-4
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
When paternally transmitted, two independent ENU-induced mutations showed reduced whole body wet weight soon after birth. The mutations were mapped to Chromosome 9 (Chr 9) between the markers D9Mit208 and D9Mft215. Their map position and imprinted status suggested that they might alter RAS protein-specific guanine nucleotide releasing factor 1 expression. Both mutations introduced premature chain termination codons into the coding sequence of Rasgrf1, and no Ras-GRF1 protein was detected in the brain. The GENA53 line had a C to T transition at nucleotide 2137, and the line GENA37 had a T to A transversion at nucleotide 3552 of the cDNA sequence. Mutant mice had near normal body weight at birth, but their weight started to lag behind that of wild-type littermates during the first week, and they were about 15% lighter as adults.
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收藏
页码:495 / 505
页数:11
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