Research Highlights | Nature Genetics

Research Highlights | Nature Genetics


Play all audios:

Loading...

Access through your institution Buy or subscribe HETEROCHRONIC CONTROL OF AGING IN WORMS In _Caenorhabditis elegans_, the microRNA (miRNA) _lin-4_ and its regulatory target _lin-14_ are


heterochronic genes that regulate the timing of larval transitions during development. Michelle Boehm and Frank Slack (_Science_ 310, 1954–1957; 2005) now show that the same two genes


function in adult worms to regulate life span and aging. The authors found that worms with loss of _lin-4_ or gain of _lin-14_ function had shortened life spans, whereas worms overexpressing


_lin-4_ or lacking _lin-14_ function had extended life spans. The mutants also showed reciprocal changes in sensitivity to heat shock and accumulation of intestinal autofluorescence, two


well-studied markers of aging in worms. Notably, interfering with adult _lin-14_ function recapitulated the extended life span phenotype and partially rescued the shortened life span of


_lin-4_ mutants. The authors further showed that _lin-4_ and _lin-14_ interacted genetically with components of the _daf-2/daf-16_ insulin-like signaling pathway, which has a conserved role


in regulating life span across multiple species. The results suggest that heterochronic genes such as _lin-4_ and _lin-14_ may influence organismal aging in a manner analogous to their roles


in regulating the timing of key transitions during larval development. _KV_ This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through your


institution Subscribe to this journal Receive 12 print issues and online access $209.00 per year only $17.42 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access


to full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read


our FAQs * Contact customer support RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Research Highlights. _Nat Genet_ 38, 147 (2006).


https://doi.org/10.1038/ng0206-147 Download citation * Issue Date: February 2006 * DOI: https://doi.org/10.1038/ng0206-147 SHARE THIS ARTICLE Anyone you share the following link with will be


able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing


initiative