Department of Biotechnology
inStem (Institute for Stem Cell Science and Regenerative Medicine)

The primary cilium dampens proliferative signaling and represses a G2/M transcriptional network in quiescent myoblasts.

Publication Type

Journal Article

Date of Publication

April 15, 2020

Journal

BMC molecular and cell biology

Volume/Issue

21/1

ISSN

2661-8850

Reversible cell cycle arrest (quiescence/G0) is characteristic of adult stem cells and is actively controlled at multiple levels. Quiescent cells also extend a primary cilium, which functions as a signaling hub. Primary cilia have been shown to be important in multiple developmental processes, and are implicated in numerous developmental disorders. Although the association of the cilium with G0 is established, the role of the cilium in the control of the quiescence program is still poorly understood.

Alternate Journal

BMC Mol Cell Biol

PubMed ID

32293249

PubMed Central ID

PMC7161131

Authors

Nisha Venugopal
Ananga Ghosh
Hardik Gala
Ajoy Aloysius
Neha Vyas
Jyotsna Dhawan

Keywords

Adaptor Proteins, Signal Transducing
Gene Regulatory Networks
Cell Cycle Checkpoints
Cell Cycle Proteins
Centrosome
Myoblasts, Skeletal
Tumor Suppressor Proteins
Animals
Cell Differentiation
Signal Transduction
Cell Proliferation
Mice
Transcription Factors
Cell Line
Cilia
Cell Cycle