A developmental transcriptomic analysis of Pax1 and Pax9 in embryonic intervertebral disc development

Author:

Sivakamasundari V.1,Kraus Petra2,Sun Wenjie3,Hu Xiaoming3,Lim Siew Lan3,Prabhakar Shyam3,Lufkin Thomas2ORCID

Affiliation:

1. The Jackson Laboratory for Genomic Medicine, 10 Discovery Drive, Farmington, CT 06030 USA

2. Department of Biology, Clarkson University, 8 Clarkson Avenue, Potsdam, NY 13699 USA

3. Genome Institute of Singapore, 60 Biopolis Street, 138672 Singapore

Abstract

Pax1 and Pax9 play redundant, synergistic functions in the patterning and differentiation of the sclerotomal cells that give rise to the vertebral bodies and intervertebral discs (IVD) of the axial skeleton. They are conserved in mice and humans, whereby mutations/deficiency of human PAX1/PAX9 have been associated with kyphoscoliosis. By combining cell-type specific transcriptome and ChIP-sequencing data, we identified the roles of Pax1/Pax9 in cell proliferation, cartilage development and collagen fibrillogenesis, which are vital in early IVD morphogenesis. Pax1 is up-regulated in the absence of Pax9, while Pax9 is unaffected by the loss of Pax1/Pax9. We identified the targets compensated by a single- or double-copy of Pax9. They positively regulate many of the cartilage genes known to be regulated by Sox5/Sox6/Sox9 and are connected to Sox5/Sox6 by a negative feedback loop. Pax1/Pax9 are intertwined with BMP and TGF-B pathways and we propose they initiate expression of chondrogenic genes during early IVD differentiation and subsequently become restricted to the outer annulus by the negative feedback mechanism. Our findings highlight how early IVD development is regulated spatio-temporally and have implications for understanding kyphoscoliosis.

Funder

Agency for Science, Technology and Research

Bayard and Virginia Clarkson Endowment

Publisher

The Company of Biologists

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

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