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J. Biol. Chem., Vol. 266, Issue 30, 19878-19881, Oct, 1991
LQ Wang, R Balakir and WE Horton Jr
Collagen II is synthesized at high levels by differentiated chondrocytes. A
620-base pair DNA sequence in the first intron of the rat collagen II gene
was previously determined to have chondrocyte- specific enhancer activity.
Using mobility shift assays, we have defined a decamer sequence,
5'-CACAATGCAT-3', in the middle of the enhancer that binds a protein or
protein complex expressed by chondrocytes but not by NIH3T3 cells or L2 rat
fibroblasts. This protein was also induced during the differentiation of
limb bud mesenchymal cells into chondrocytes. Mutational analyses, coupled
with both in vitro binding studies and direct assays of enhancer activity
following transfection into cells, demonstrated that this sequence is
involved in the binding of the chondrocyte nuclear protein(s) and is
necessary for the enhancer activity. This sequence has homology to the
consensus binding sequence for helix-loop-helix transcription factors.
Identification of a cis-acting sequence in the collagen II enhancer required for chondrocyte expression and the binding of a chondrocyte nuclear factor
Laboratory of Biological Chemistry, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224.
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