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PMID: 15301607 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Haploinsufficiency of Dyrk1A in mice leads to specific alterations in the development and regulation of motor activity.

Behavioral neuroscience ·Vol. 118 ·No. 4 ·2004-08-00 ·Pages 815-21

Fotaki V, Martínez De Lagrán M, Estivill X, Arbonés M, Dierssen M

Abstract

DYRK1A is a protein kinase proposed to be involved in neurogenesis. Gene-targeting disruption of Dyrk1A in mice leads to decreased body and brain size, with no severe disturbance of behavior. In this study, the authors focused on the motor profile of Dyrk1A(+/-) mice. These mice presented impairment of neuromotor development with decreased activity, suggesting a physiological role of Dyrk1A in the maturation of the neuromotor system. In the adult, a marked hypoactivity and alteration of specific motor parameters were detected. These results are in agreement with the significant expression of Dyrk1A in structures related to motor function and support a role of Dyrk1A in the control of motor function.

MeSH Terms
Age Factors Analysis of Variance Animals Animals, Newborn Exploratory Behavior/physiology Hand Strength/physiology Haplotypes Mice Mice, Inbred Strains Mice, Transgenic Motor Activity/physiology Protein Serine-Threonine Kinases/deficiency,genetics,physiology Protein-Tyrosine Kinases/deficiency,genetics,physiology Psychomotor Performance/physiology Reaction Time/physiology Walking/physiology
Chemicals
Dyrk kinase Protein-Tyrosine Kinases Protein Serine-Threonine Kinases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Fotaki V
Genetics and Disease Program, Genomic Regulation Center, Barcelona, Spain.
Martínez De Lagrán M
Estivill X
Arbonés M
Dierssen M
Article Info
Journal
Behavioral neuroscience
Abbr.
Behav Neurosci
ISSN
0735-7044
Published
2004-08-00
Pages
815-21
Language
English
Region
United States
NLM ID
8302411
Subset
IM
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