Different circadian expression of major matrix-related genes in various types of cartilage: modulation by light–dark conditions

KK Honda, T Kawamoto, HR Ueda… - The journal of …, 2013 - academic.oup.com
KK Honda, T Kawamoto, HR Ueda, A Nakashima, T Ueshima, RG Yamada, M Nishimura…
The journal of biochemistry, 2013academic.oup.com
We screened circadian-regulated genes in rat cartilage by using a DNA microarray analysis.
In rib growth-plate cartilage, numerous genes showed statistically significant circadian
mRNA expression under both 12: 12 h light–dark and constant darkness conditions. Type II
collagen and aggrecan genes—along with several genes essential for post-translational
modifications of collagen and aggrecan, including prolyl 4-hydroxylase 1, lysyl oxidase, lysyl
oxidase-like 2 and 3′-phosphoadenosine 5′-phosphosulphate synthase 2—showed the …
Abstract
We screened circadian-regulated genes in rat cartilage by using a DNA microarray analysis. In rib growth-plate cartilage, numerous genes showed statistically significant circadian mRNA expression under both 12:12 h light–dark and constant darkness conditions. Type II collagen and aggrecan genes—along with several genes essential for post-translational modifications of collagen and aggrecan, including prolyl 4-hydroxylase 1, lysyl oxidase, lysyl oxidase-like 2 and 3′-phosphoadenosine 5′-phosphosulphate synthase 2—showed the same circadian phase. In addition, the mRNA level of SOX9, a master transcription factor for the synthesis of type II collagen and aggrecan, has a similar phase of circadian rhythms. The circadian expression of the matrix-related genes may be critical in the development and the growth of various cartilages, because similar circadian expression of the matrix-related genes was observed in hip joint cartilage. However, the circadian phase of the major matrix-related genes in the rib permanent cartilage was almost the converse of that in the rib growth-plate cartilage under light–dark conditions. We also found that half of the oscillating genes had conserved clock-regulatory elements, indicating contribution of the elements to the clock outputs. These findings suggest that the synthesis of the cartilage matrix macromolecules is controlled by cell-autonomous clocks depending upon the in vivo location of cartilage.
Oxford University Press