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

作者信息

Clapcott Steven J, Peters Josephine, Orban Paul C, Brambilla Riccardo, Graham Chris F

机构信息

Zoology Department, South Parks Road, Oxford, OX1 3PS, UK.

出版信息

Mamm Genome. 2003 Aug;14(8):495-505. doi: 10.1007/s00335-002-2258-4.

DOI:10.1007/s00335-002-2258-4
PMID:12925882
Abstract

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 D9Mit215. 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.

摘要

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本文引用的文献

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