Affiliation:
1. Department of Cell Biology and Orthopaedic Research Center, Lerner Research Institute, Cleveland Clinic, Cleveland, Ohio 44195
Abstract
ABSTRACT
The Sry-related high-mobility-group box transcription factor Sox9 recruits the redundant L-Sox5 and Sox6 proteins to effect chondrogenesis, but the mode of action of the trio remains unclear. We identify here a highly conserved 359-bp sequence 10 kb upstream of the
Agc1
gene for aggrecan, a most essential cartilage proteoglycan and key marker of chondrocyte differentiation. This sequence directs expression of a minimal promoter in both embryonic and adult cartilage in transgenic mice, in a manner that matches
Agc1
expression. The chondrogenic trio is required and sufficient to mediate the activity of this enhancer. It acts directly, Sox9 binding to a critical
cis
-acting element and L-Sox5/Sox6 binding to three additional elements, which are cooperatively needed. Upon binding to their specific sites, L-Sox5/Sox6 increases the efficiency of Sox9 binding to its own recognition site and thereby robustly potentiates the ability of Sox9 to activate the enhancer. L-Sox5/Sox6 similarly secures Sox9 binding to
Col2a1
(encoding collagen-2) and other cartilage-specific enhancers. This study thus uncovers critical
cis
-acting elements and transcription factors driving
Agc1
expression in cartilage and increases understanding of the mode of action of the chondrogenic Sox trio.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
Cited by
247 articles.
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