HOX gene expression in the developing human spine

Positional coding along the anterior-posterior axis is regulated by HOX genes, whose 3' to 5' expression correlates with location along this axis. The precise utilisation of HOX genes in different human cell types is not fully understood. Here, we use single-cell and spatial-transcriptomics, along with in-situ sequencing, to create a developmental atlas of the human fetal spine. We analyse HOX gene expression across cell types during development, finding that neural-crest derivatives unexpectedly retain the anatomical HOX code of their origin while also adopting the code of their destination. This trend is confirmed across multiple organs. In the axial plane of the spinal cord, we find distinct patterns in the ventral and dorsal domains, providing insights into motor pool organisation and loss of collinearity in HOXB genes. Our findings shed new light on HOX gene expression in the developing spine, highlighting a HOX gene 'source code' in neural-crest cell derivatives.

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Publication Details

Journal
Nature Communications
Published
2024-11-20
DOI
https://doi.org/10.1038/s41467-024-54187-0
Citations
16
Primary Topic
Developmental Biology and Gene Regulation
Type
article
Field-Weighted Citation Impact
3.74

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article

HOX gene expression in the developing human spine

Pavel Mazin, Omer Ali Bayraktar, John E. Lawrence, Lira Mamanova et al.
16 citations
Nature Communications
Developmental Biology and Gene Regulation
3.74
article

HOX gene expression in the developing human spine

Pavel Mazin, Omer Ali Bayraktar, John E. Lawrence, Lira Mamanova, Sarah Amalia Teichmann, Alice Piapi, Liam Bolt, Elena Prigmore, Inga Usher, Tong Li, Adrienne M. Flanagan, Laura Richardson, Kenny S. Roberts, Petra Balogh, Sam Behjati, Nathaniel D. Anderson, Xiaoling He, Roger A. Barker, Matthew D. Young, Elizabeth J. Tuck
article en
16 citations

Abstract

Positional coding along the anterior-posterior axis is regulated by HOX genes, whose 3' to 5' expression correlates with location along this axis. The precise utilisation of HOX genes in different human cell types is not fully understood. Here, we use single-cell and spatial-transcriptomics, along with in-situ sequencing, to create a developmental atlas of the human fetal spine. We analyse HOX gene expression across cell types during development, finding that neural-crest derivatives unexpectedly retain the anatomical HOX code of their origin while also adopting the code of their destination. This trend is confirmed across multiple organs. In the axial plane of the spinal cord, we find distinct patterns in the ventral and dorsal domains, providing insights into motor pool organisation and loss of collinearity in HOXB genes. Our findings shed new light on HOX gene expression in the developing spine, highlighting a HOX gene 'source code' in neural-crest cell derivatives.

Nature CommunicationsVol. 15(1)
Wellcome/MRC Cambridge Stem Cell Institute (GB), University of Cambridge (GB), Great Ormond Street Hospital (GB), Cambridge University Hospitals NHS Foundation Trust (GB), Wellcome Sanger Institute (GB), Royal National Orthopaedic Hospital (GB), Addenbrooke's Hospital (GB), University College London (GB)
Wellcome, Wellcome Trust, Medical Research Council
Openalex Percentile: Top 6%
Developmental Biology and Gene Regulation
3.74
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