Germ-cell loss extends C. elegans life span through regulation of DAF-16 by kri-1 and lipophilic-hormone signaling.

Abstract:

:In C. elegans, removing the germ cells extends life span by triggering the nuclear localization and activation of the DAF-16/FOXO transcription factor in the intestine. In this study, we identify and analyze genes required for germline removal to extend life span. We find that the reproductive system communicates with the intestine through lipophilic-hormone signaling and that a gene called kri-1 is likely to act in the intestine to promote DAF-16 nuclear localization in response to this signal. This lipophilic-signaling pathway and kri-1 are not required for DAF-16's nuclear localization and life-span extension in animals with decreased insulin/IGF-1 signaling. Thus, this pathway specifically enables the integration of cues from the reproductive system with central DAF-16-activation pathways to influence the aging of the animal.

journal_name

Cell

journal_title

Cell

authors

Berman JR,Kenyon C

doi

10.1016/j.cell.2006.01.039

subject

Has Abstract

pub_date

2006-03-10 00:00:00

pages

1055-68

issue

5

eissn

0092-8674

issn

1097-4172

pii

S0092-8674(06)00237-6

journal_volume

124

pub_type

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