Literature DB >> 10753520

Hox C cluster genes are dispensable for overall body plan of mouse embryonic development.

H Suemori1, S Noguchi.   

Abstract

Hox genes encode transcription factors which provide positional information during morphogenesis along the body axis; genetic interaction among Hox genes is thought to be necessary for correct pattern formation. One of the most curious features of the 39 vertebrate Hox genes is that they form four clusters each composed of several genes paralogous between clusters. This raises the question are all four clusters necessary for the development of vertebrates and, if so, what is the function of each cluster? To provide an answer to this question, we prepared Hox C cluster null mice utilizing the Cre-loxP system. Hox C cluster null mice, lacking all nine Hox C genes, die at the time of birth; however, the mutant pups develop to this stage with minor transformations. This development shows that the Hox C genes are dispensable for the overall body plan of mouse embryogenesis. Furthermore, transformations observed in the skeletal system of the Hox C cluster null mice are milder than those observed in the Hoxc-9 null mice, providing further evidence that at least some genes within a cluster exhibit interaction functions with each other. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10753520     DOI: 10.1006/dbio.2000.9651

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  39 in total

Review 1.  Origins of anteroposterior patterning and Hox gene regulation during chordate evolution.

Authors:  T F Schilling; R D Knight
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2001-10-29       Impact factor: 6.237

2.  Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs.

Authors:  John L Rinn; Michael Kertesz; Jordon K Wang; Sharon L Squazzo; Xiao Xu; Samantha A Brugmann; L Henry Goodnough; Jill A Helms; Peggy J Farnham; Eran Segal; Howard Y Chang
Journal:  Cell       Date:  2007-06-29       Impact factor: 41.582

Review 3.  Molecular basis for skeletal variation: insights from developmental genetic studies in mice.

Authors:  C Kappen; A Neubüser; R Balling; R Finnell
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2007-12

Review 4.  Physiological roles of long noncoding RNAs: insight from knockout mice.

Authors:  Lingjie Li; Howard Y Chang
Journal:  Trends Cell Biol       Date:  2014-07-09       Impact factor: 20.808

5.  Reshuffling genomic landscapes to study the regulatory evolution of Hox gene clusters.

Authors:  Patrick Tschopp; Nadine Fraudeau; Frédérique Béna; Denis Duboule
Journal:  Proc Natl Acad Sci U S A       Date:  2011-06-13       Impact factor: 11.205

6.  Axial Hox9 activity establishes the posterior field in the developing forelimb.

Authors:  Ben Xu; Deneen M Wellik
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-07       Impact factor: 11.205

7.  Changes in Hox genes' structure and function during the evolution of the squamate body plan.

Authors:  Nicolas Di-Poï; Juan I Montoya-Burgos; Hilary Miller; Olivier Pourquié; Michel C Milinkovitch; Denis Duboule
Journal:  Nature       Date:  2010-03-04       Impact factor: 49.962

8.  Recruitment of 5' Hoxa genes in the allantois is essential for proper extra-embryonic function in placental mammals.

Authors:  Martina Scotti; Marie Kmita
Journal:  Development       Date:  2012-01-04       Impact factor: 6.868

Review 9.  Review of the Genetic Basis of Jaw Malformations.

Authors:  Mairaj K Ahmed; Xiaoqian Ye; Peter J Taub
Journal:  J Pediatr Genet       Date:  2016-10-12

10.  Axial and appendicular skeletal transformations, ligament alterations, and motor neuron loss in Hoxc10 mutants.

Authors:  Sirkka Liisa Hostikka; Jun Gong; Ellen M Carpenter
Journal:  Int J Biol Sci       Date:  2009-06-03       Impact factor: 6.580

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