Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published April 1, 2015 | Supplemental Material
Journal Article Open

Znf385C mediates a novel p53-dependent transcriptional switch to control timing of facial bone formation

Abstract

Jaw formation involves an intricate series of molecular events, whereby a chondrogenic scaffold precedes osteogenesis. The mechanisms coupling timing of cartilage maturation to onset of bone differentiation are poorly understood, particularly for neural crest-derived bones of the head. Here we present a novel zebrafish gene/protein-trap Citrine-fusion line that reveals transient expression of the zinc-finger protein Znf385C in maturing chondrocytes of the jaw. Functional analysis shows that loss of Znf385C disrupts a distinct peak of p21^(cip1/waf1) expression in the chondrocytes, as well as causes premature ossification of the zebrafish jaw. We find that Znf385C is expressed as two splice variants which act differentially to activate p21^(cip1/waf1) and/or interact with p53 in subcellular compartments. Taken together, the results suggest that Znf385C acts as a developmental switch for p53 function that modulates cell cycle arrest of chondrocytes and regulates timing of jaw cartilage maturation and ossification.

Additional Information

© 2015 Elsevier Inc. Received 10 January 2015, Accepted 12 January 2015, Available online 27 January 2015. We thank Dr. Tatjana Sauka-Spengler for valuable discussions, Dr. Sujata Bhattacharyya for comments on the manuscript, and Dr. Le Trinh and Dr. Scott Fraser for helpful advice. We thank Leigh Ann Fletcher, Kwok Su and David Mayorga for fish care; Neha Das Messenger, Ilana Solomon and Joyce De Leon for technical support; and Dr. Robert Kelsh for sharing the Tg(-4.9sox10:EGFP) line. Financial support: T.H.H. was supported by a Pew Latin American Fellowship in the Biomedical Sciences and by a California Institute for Regenerative Medicine Training Grant (T2-00006). This work was supported by NIH grants HD037105 and HG004071 (M.E.B). Author contributions: T.H.H. designed and performed experiments, analyzed data, and wrote the manuscript. D.E.S.K. performed experiments, analyzed data, and edited the manuscript. M.E.B. supervised the work including helping with experimental design, data, analysis, and manuscript preparation. Ethics statement for animal experimentation This study was performed in strict accordance with the guidelines in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. All of the animals were handled according to approved Institutional Animal Care and Use Committee (IACUC) protocol at the California Institute of Technology.

Attached Files

Supplemental Material - mmc1.pdf

Files

mmc1.pdf
Files (442.4 kB)
Name Size Download all
md5:d1b1bcf494f2a7ec834affaf101c4051
442.4 kB Preview Download

Additional details

Created:
August 22, 2023
Modified:
October 20, 2023