TY - JOUR
T1 - Identification and characterization of an insulin receptor substrate 4-interacting protein in rat brain
T2 - Implications for longevity
AU - Chiba, Takuya
AU - Inoue, Daisuke
AU - Mizuno, Aya
AU - Komatsu, Toshimitsu
AU - Fujita, Satoshi
AU - Kubota, Haruaki
AU - Luisa Tagliaro, Maria
AU - Park, Seongjoon
AU - Trindade, Lucas Siqueira
AU - Hayashida, Takahiro
AU - Hayashi, Hiroko
AU - Yamaza, Haruyoshi
AU - Higami, Yoshikazu
AU - Shimokawa, Isao
N1 - Funding Information:
We thank Dr. Yoshihiro Ohta (Tokyo University of Agriculture and Technology) for providing us GT1-7 cells established by Dr. Weiner. We are grateful to the staff at Biomedical Research Center at Center for Frontier Life Sciences, Nagasaki University for their technical assistance and animal care. We also thank Yutaka Araki and Yuko Moriyama for technical assistance. This work was supported in part by Grant-in-Aid for Young Scientists (B) from the Japan Society for the Promotion of Science 17790269 (TC).
PY - 2009/3
Y1 - 2009/3
N2 - The hypothalamus is organized as a collection of distinct, autonomously active nuclei that regulate discrete functions, such as feeding activity and metabolism. We used suppression subtractive hybridization (SSH) to identify genes that are enriched in the hypothalamus of the rat brain. We screened a subtractive library of 160 clones, and 4 genes that were predominantly expressed in the hypothalamus, compared to other brain regions. The mRNA for a member of the WD-repeat family of proteins, WDR6, was abundantly expressed in the hypothalamus, and we found that WDR6 interacted with insulin receptor substrate 4 (IRS-4) in the rat brain. Interestingly, WDR6 gene expression in the hypothalamic arcuate nucleus was decreased by caloric restriction, and in growth hormone (GH)-antisense transgenic rats, both of which are associated with an increased life span. Insulin-like growth factor (IGF)-I and insulin treatment increased WDR6 gene expression in mouse hypothalamus-derived GT1-7 cells. Our results might suggest that WDR6 participates in insulin/IGF-I signaling and the regulation of feeding behavior and longevity in the brain.
AB - The hypothalamus is organized as a collection of distinct, autonomously active nuclei that regulate discrete functions, such as feeding activity and metabolism. We used suppression subtractive hybridization (SSH) to identify genes that are enriched in the hypothalamus of the rat brain. We screened a subtractive library of 160 clones, and 4 genes that were predominantly expressed in the hypothalamus, compared to other brain regions. The mRNA for a member of the WD-repeat family of proteins, WDR6, was abundantly expressed in the hypothalamus, and we found that WDR6 interacted with insulin receptor substrate 4 (IRS-4) in the rat brain. Interestingly, WDR6 gene expression in the hypothalamic arcuate nucleus was decreased by caloric restriction, and in growth hormone (GH)-antisense transgenic rats, both of which are associated with an increased life span. Insulin-like growth factor (IGF)-I and insulin treatment increased WDR6 gene expression in mouse hypothalamus-derived GT1-7 cells. Our results might suggest that WDR6 participates in insulin/IGF-I signaling and the regulation of feeding behavior and longevity in the brain.
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U2 - 10.1016/j.neurobiolaging.2007.07.008
DO - 10.1016/j.neurobiolaging.2007.07.008
M3 - Article
C2 - 17720279
AN - SCOPUS:58549118766
SN - 0197-4580
VL - 30
SP - 474
EP - 482
JO - Neurobiology of Aging
JF - Neurobiology of Aging
IS - 3
ER -