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Scleraxis is Required for Maturation of Tissue Domains for Proper Integration of the Musculoskeletal System

Overview
Journal Sci Rep
Specialty Science
Date 2017 Mar 23
PMID 28327634
Citations 54
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Abstract

Scleraxis (Scx) is a basic helix-loop-helix transcription factor that is expressed persistently in tendons/ligaments, but transiently in entheseal cartilage. In this study, we generated a novel Scx knock-in (KI) allele, by in-frame replacement of most of Scx exon 1 with Cre recombinase (Cre), to drive Cre expression using Scx promoter and to inactivate the endogenous Scx. Reflecting the intensity and duration of endogenous expression, Cre-mediated excision occurs in tendinous and ligamentous tissues persistently expressing Scx. Expression of tenomodulin, a marker of mature tenocytes and ligamentocytes, was almost absent in tendons and ligaments of Scx KI mice lacking Scx to indicate defective maturation. In homozygotes, the transiently Scx-expressing entheseal regions such as the rib cage, patella cartilage, and calcaneus were small and defective and cartilaginous tuberosity was missing. Decreased Sox9 expression and phosphorylation of Smad1/5 and Smad3 were also observed in the developing entheseal cartilage, patella, and deltoid tuberosity of Scx KI mice. These results highlighted the functional importance of both transient and persistent expression domains of Scx for proper integration of the musculoskeletal components.

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References
1.
Dex S, Lin D, Shukunami C, Docheva D . Tenogenic modulating insider factor: Systematic assessment on the functions of tenomodulin gene. Gene. 2016; 587(1):1-17. PMC: 4897592. DOI: 10.1016/j.gene.2016.04.051. View

2.
Havis E, Bonnin M, Olivera-Martinez I, Nazaret N, Ruggiu M, Weibel J . Transcriptomic analysis of mouse limb tendon cells during development. Development. 2014; 141(19):3683-96. DOI: 10.1242/dev.108654. View

3.
Shi Y, Massague J . Mechanisms of TGF-beta signaling from cell membrane to the nucleus. Cell. 2003; 113(6):685-700. DOI: 10.1016/s0092-8674(03)00432-x. View

4.
Blitz E, Viukov S, Sharir A, Shwartz Y, Galloway J, Pryce B . Bone ridge patterning during musculoskeletal assembly is mediated through SCX regulation of Bmp4 at the tendon-skeleton junction. Dev Cell. 2010; 17(6):861-73. PMC: 3164485. DOI: 10.1016/j.devcel.2009.10.010. View

5.
Brown D, Wagner D, Li X, Richardson J, Olson E . Dual role of the basic helix-loop-helix transcription factor scleraxis in mesoderm formation and chondrogenesis during mouse embryogenesis. Development. 1999; 126(19):4317-29. DOI: 10.1242/dev.126.19.4317. View