English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT
  LIN-28 balances longevity and germline stem cell number in Caenorhabditis elegans through let-7/AKT/DAF-16 axis

Wang, D., Hou, L., Nakamura, S., Su, M., Li, F., Chen, W., et al. (2017). LIN-28 balances longevity and germline stem cell number in Caenorhabditis elegans through let-7/AKT/DAF-16 axis. Aging Cell, 2017 Feb(16(1)), 113-124. doi:10.1111/acel.12539.

Item is

Files

show Files

Locators

show
hide
Description:
-
OA-Status:
Not specified

Creators

show
hide
 Creators:
Wang, D., Author
Hou, L., Author
Nakamura, S.1, Author           
Su, M., Author
Li, F., Author
Chen, W., Author
Yan, Y., Author
Green, C. D., Author
Chen, D., Author
Zhang, H., Author
Antebi, A.1, Author           
Han, J. J., Author
Affiliations:
1Department Antebi - Molecular Genetics of Ageing, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_1942285              

Content

show
hide
Free keywords: Caenorhabditis elegans Daf-16 Lin-28 let-7 longevity reproduction
 Abstract: The RNA-binding protein LIN-28 was first found to control developmental timing in Caenorhabditis elegans. Later, it was found to play important roles in pluripotency, metabolism, and cancer in mammals. Here we report that a low dosage of lin-28 enhanced stress tolerance and longevity, and reduced germline stem/progenitor cell number in C. elegans. The germline LIN-28-regulated microRNA let-7 was required for these effects by targeting akt-1/2 and decreasing their protein levels. AKT-1/2 and the downstream DAF-16 transcription factor were both required for the lifespan and germline stem cell effects of lin-28. The pathway also mediated dietary restriction induced lifespan extension and reduction in germline stem cell number. Thus, the LIN-28/let-7/AKT/DAF-16 axis we delineated here is a program that plays an important role in balancing reproduction and somatic maintenance and their response to the environmental energy level-a central dogma of the 'evolutionary optimization' of resource allocation that modulates aging.

Details

show
hide
Language(s):
 Dates: 2016-10-132017-10-11
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1111/acel.12539
ISSN: 1474-9718
 Degree: -

Event

show

Legal Case

show

Project information

show

Source 1

show
hide
Title: Aging Cell
  Alternative Title : Aging cell
Source Genre: Journal
 Creator(s):
Affiliations:
Publ. Info: -
Pages: - Volume / Issue: 2017 Feb (16(1)) Sequence Number: - Start / End Page: 113 - 124 Identifier: -