Home
Scholarly Works
picd-1, a gene that encodes CABIN1...
Journal article

picd-1, a gene that encodes CABIN1 domain-containing protein, interacts with pry-1/Axin to regulate multiple processes in Caenorhabditis elegans

Abstract

ABSTRACT AXIN family members control diverse biological processes in eukaryotes. As a scaffolding protein, AXIN facilitates interactions between cellular components and provides specificity to signaling pathways. Despite its crucial roles in metazoans and discovery of a large number of family members, the mechanism of AXIN function is not very well understood. The C. elegans AXIN homolog PRY-1 provides a powerful tool to identify interacting genes and downstream effectors that function in a conserved manner to regulate AXIN-mediated signaling. Previous work demonstrated pry-1 ’s essential role in developmental processes such as reproductive system, seam cells, and a P lineage cell P11.p. More recently, our lab carried out a transcriptome profiling of pry-1 mutant and uncovered the essential role of the gene in lipid metabolism, stress response, and aging. In this study, we have extended the work on pry-1 by reporting a novel interacting gene picd-1 ( p ry-1 - i nteracting C ABIN1 d omain containing). Our findings have revealed that picd-1 plays an essential role in C. elegans and is involved in several pry-1 -mediated processes including regulation of stress response and lifespan maintenance. In support of this, picd-1 expression overlaps with pry-1 in multiple tissues throughout the lifespan of animals. Further experiments showed that picd-1 inhibits CREB-regulated transcriptional coactivator homolog CRTC-1 function, which promotes longevity in a calcineurin-dependent manner. These data provide evidence for an essential role of the CABIN1 domain protein PICD-1 in mediating PRY-1 signaling in C. elegans .

Authors

Mallick A; Taylor SKB; Mehta S; Gupta BP

Journal

, , ,

Publisher

Cold Spring Harbor Laboratory

Publication Date

September 28, 2021

DOI

10.1101/2021.09.27.462077

ISSN

2692-8205
View published work (Non-McMaster Users)

Contact the Experts team