TY - JOUR
T1 - Large-scale mutagenesis and phenotypic screens for the nervous system and behavior in mice
AU - Vitaterna, Martha Hotz
AU - Pinto, Lawrence H.
AU - Takahashi, Joseph S.
N1 - Funding Information:
This work was supported by the NIH cooperative agreement U01 MH 61915, and the Zaffaroni Foundation. J.S.T. is an Investigator in the Howard Hughes Medical Institute.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2006/4
Y1 - 2006/4
N2 - Significant developments have occurred in our understanding of the mammalian genome thanks to informatics, expression profiling and sequencing of the human and rodent genomes. However, although these facets of genomic analysis are being addressed, analysis of in vivo gene function remains a formidable task. Evaluation of the phenotype of mutants provides powerful access to gene function, and this approach is particularly relevant to the nervous system and behavior. Here, we discuss the complementary mouse genetic approaches of gene-driven, targeted mutagenesis and phenotype-driven, chemical mutagenesis. We highlight an NIH-supported large-scale effort to use phenotype-driven mutagenesis screens to identify mouse mutants with neural and behavioral alterations. Such single-gene mutations can then be used for gene identification using positional candidate gene-cloning methods.
AB - Significant developments have occurred in our understanding of the mammalian genome thanks to informatics, expression profiling and sequencing of the human and rodent genomes. However, although these facets of genomic analysis are being addressed, analysis of in vivo gene function remains a formidable task. Evaluation of the phenotype of mutants provides powerful access to gene function, and this approach is particularly relevant to the nervous system and behavior. Here, we discuss the complementary mouse genetic approaches of gene-driven, targeted mutagenesis and phenotype-driven, chemical mutagenesis. We highlight an NIH-supported large-scale effort to use phenotype-driven mutagenesis screens to identify mouse mutants with neural and behavioral alterations. Such single-gene mutations can then be used for gene identification using positional candidate gene-cloning methods.
UR - http://www.scopus.com/inward/record.url?scp=33645961290&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33645961290&partnerID=8YFLogxK
U2 - 10.1016/j.tins.2006.02.006
DO - 10.1016/j.tins.2006.02.006
M3 - Review article
C2 - 16519954
AN - SCOPUS:33645961290
SN - 0166-2236
VL - 29
SP - 233
EP - 240
JO - Trends in Neurosciences
JF - Trends in Neurosciences
IS - 4
ER -