Literature DB >> 23940085

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

Kiyomasa K Honda1, Takeshi Kawamoto, Hiroki R Ueda, Ayumu Nakashima, Taichi Ueshima, Rikuhiro G Yamada, Masahiro Nishimura, Ryo Oda, Shigeo Nakamura, Tomoko Kojima, Mitsuhide Noshiro, Katsumi Fujimoto, Seiichi Hashimoto, Yukio Kato.   

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.

Entities:  

Keywords:  cartilage; circadian rhythm; clock; gene expression

Mesh:

Substances:

Year:  2013        PMID: 23940085     DOI: 10.1093/jb/mvt068

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


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