<i>ist-1/IRS1</i> affects L1 starvation resistance in <i>daf-16/FoxO-</i> dependent and independent fashion.

dc.contributor.author

Chen, Jingxian

dc.contributor.author

Scheiner, Ainsley R

dc.contributor.author

Falsztyn, Ivan B

dc.contributor.author

Baugh, L Ryan

dc.date.accessioned

2025-08-01T16:17:16Z

dc.date.available

2025-08-01T16:17:16Z

dc.date.issued

2025-01

dc.description.abstract

The mammalian IRS1 gene is an important adaptor for the insulin and insulin-like growth factor receptors, but its sole homolog in the nematode C. elegans , ist-1 , has received relatively little attention. We show that ist-1 /IRS1 has modest effects on L1 starvation resistance, with two null mutants increasing larval growth and reproduction after recovery from extended L1 arrest. ist-1 /IRS1 mutants increase nuclear localization of DAF-16 /FoxO, a critical effector of insulin/IGF signaling, in starved L1 larvae, consistent with IST-1 /IRS1 transducing DAF-2 /IGFR signaling. However, epistasis analysis suggests that ist-1 /IRS1 also functions independently of daf-16 /FoxO , suggesting additional, novel function.

dc.identifier.issn

2578-9430

dc.identifier.issn

2578-9430

dc.identifier.uri

https://hdl.handle.net/10161/33055

dc.language

eng

dc.relation.ispartof

microPublication biology

dc.relation.isversionof

10.17912/micropub.biology.001648

dc.rights.uri

https://creativecommons.org/licenses/by-nc/4.0

dc.title

<i>ist-1/IRS1</i> affects L1 starvation resistance in <i>daf-16/FoxO-</i> dependent and independent fashion.

dc.type

Journal article

duke.contributor.orcid

Baugh, L Ryan|0000-0003-2148-5492

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Trinity College of Arts & Sciences

pubs.organisational-group

Basic Science Departments

pubs.organisational-group

Cell Biology

pubs.organisational-group

Biology

pubs.organisational-group

Duke Regeneration Center

pubs.publication-status

Published

pubs.volume

2025

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