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PMID: 17626057 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Hox patterning of the vertebrate rib cage.

Development (Cambridge, England) ·Vol. 134 ·No. 16 ·2007-08-00 ·Pages 2981-9

McIntyre DC, Rakshit S, Yallowitz AR, Loken L, Jeannotte L, Capecchi MR, Wellik DM

Abstract

Unlike the rest of the axial skeleton, which develops solely from somitic mesoderm, patterning of the rib cage is complicated by its derivation from two distinct tissues. The thoracic skeleton is derived from both somitic mesoderm, which forms the vertebral bodies and ribs, and from lateral plate mesoderm, which forms the sternum. By generating mouse mutants in Hox5, Hox6 and Hox9 paralogous group genes, along with a dissection of the Hox10 and Hox11 group mutants, several important conclusions regarding the nature of the ;Hox code' in rib cage and axial skeleton development are revealed. First, axial patterning is consistently coded by the unique and redundant functions of Hox paralogous groups throughout the axial skeleton. Loss of paralogous function leads to anterior homeotic transformations of colinear regions throughout the somite-derived axial skeleton. In the thoracic region, Hox genes pattern the lateral plate-derived sternum in a non-colinear manner, independent from the patterning of the somite-derived vertebrae and vertebral ribs. Finally, between adjacent sets of paralogous mutants, the regions of vertebral phenotypes overlap considerably; however, each paralogous group imparts unique morphologies within these regions. In all cases examined, the next-most posterior Hox paralogous group does not prevent the function of the more-anterior Hox group in axial patterning. Thus, the ;Hox code' in somitic mesoderm is the result of the distinct, graded effects of two or more Hox paralogous groups functioning in any anteroposterior location.

MeSH Terms
Animals Animals, Genetically Modified Body Patterning/genetics Bone and Bones/embryology,metabolism Gene Expression Profiling Gene Expression Regulation, Developmental Homeodomain Proteins/genetics,metabolism Mice Models, Biological Ribs/embryology,metabolism Tissue Distribution Vertebrates/genetics
Chemicals
Homeodomain Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
McIntyre Daniel C
Division of Molecular Medicine and Genetics, Department of Internal Medicine, University of Michigan Medical Center, 109 Zina Pitcher, Ann Arbor, MI 48109-2200, USA.
Rakshit Sabita
Yallowitz Alisha R
Loken Luke
Jeannotte Lucie
Capecchi Mario R
Wellik Deneen M
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2007-08-00
Epub
2007-00-11
Pages
2981-9
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NICHD NIH HHS · T32 HD007505 · United States
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