Functional characterization and immunolocalization of the transporter encoded by the life-extending gene Indy

被引:83
作者
Knauf, F
Rogina, B
Jiang, ZR
Aronson, PS
Helfand, SL
机构
[1] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[2] Humboldt Univ, Fac Med Charite, HELIOS Klin Berlin, Franz Volhard Clin,Max Delb, D-14050 Berlin, Germany
[3] Univ Connecticut, Ctr Hlth, Dept Genet & Dev Biol, Sch Med, Farmington, CT 06030 USA
关键词
D O I
10.1073/pnas.222531899
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Caloric restriction extends life span in a variety of species, highlighting the importance of energy balance in aging. A new longevity gene, Indy (for I'm not dead yet), which doubles the average life span of flies without a loss of fertility or physical activity, was postulated to extend life by affecting intermediary metabolism. We report that functional studies in Xenopus oocytes show INDY is a metabolite transporter that mediates the high-affinity, disulfonic stilbene-sensitive flux of dicarboxylates and citrate across the plasma membrane by a mechanism that is not coupled to Na+, K+, or Cl-. Immunocytochemical studies localize INDY to the plasma membrane with most prominent expression in adult fat body, oenocytes, and the basolateral region of midgut cells and show that life-extending mutations in Indy reduce INDY expression. We conclude that INDY functions as a novel sodium-independent mechanism for transporting Krebs and citric acid cycle intermediates through the epithelium of the gut and across the plasma membranes of organs involved in intermediary metabolism and storage. The life-extending effect of mutations in Indy is likely caused by an alteration in energy balance caused by a decrease in INDY transport function.
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页码:14315 / 14319
页数:5
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