Literature DB >> 17520166

Characterization of chromosomal inversion of the mouse hairy ears (Eh) mutation associated with cleft palate.

Kentaro Katayama1, Aki Furuno, Kouyou Akiyama, Takehito Tsuji, Tetsuo Kunieda.   

Abstract

The hairy ears (Eh) mutation in the mouse originated from neutron irradiation experiments and is associated with chromosomal inversion on chromosome 15. Eh/+ mice have small pinna and extra hairs on the pinna but the phenotypic features of Eh/Eh mice are unclear. In this study we found that Eh/Eh mice died shortly after birth and had a cleft palate caused by impaired growth of palate shelves. Because genes located on the breakpoints of inversion are likely to be responsible for the defects associated with chromosomal inversions, we determined the breakpoints of the Eh inversion. We used a new genetic method that uses recombinant chromosomes resulting from crossing over between two overlapping inversions to determine the breakpoints. Koa is a mouse mutation associated with inversion of chromosome 15, which partially overlaps with the Eh inversion. We made Eh +/+ Koa double heterozygotes and obtained the recombinant chromosomes possessing deletion and duplication of the regions flanked by the breakpoints of both inversions, which were generated by crossing over within the overlapped region of these inversions. By defining the deleted regions we identified the breakpoints of the Eh inversion. We then examined the expression of genes in the vicinities of the breakpoints and found ectopic expression of the Hoxc5 gene and a transcript with unknown function in the developing palate of Eh/Eh mice, which is likely to be responsible for the cleft palate.

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Year:  2007        PMID: 17520166     DOI: 10.1007/s00335-007-9015-7

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   3.224


  33 in total

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Journal:  J Clin Invest       Date:  2005-04       Impact factor: 14.808

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

Authors:  H Suemori; S Noguchi
Journal:  Dev Biol       Date:  2000-04-15       Impact factor: 3.582

5.  Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death.

Authors:  N Hagiwara; S E Klewer; R A Samson; D T Erickson; M F Lyon; M H Brilliant
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6.  Fine mapping of a region of rat chromosome 12 close to the aspermia (as) locus and comparison with the human orthologous regions.

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7.  Epidermal growth factor receptor function is necessary for normal craniofacial development and palate closure.

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Review 10.  Palate development.

Authors:  M W Ferguson
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  4 in total

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3.  Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities.

Authors:  Kentaro Katayama; Sayaka Miyamoto; Aki Furuno; Kouyou Akiyama; Sakino Takahashi; Hiroetsu Suzuki; Takehito Tsuji; Tetsuo Kunieda
Journal:  BMC Genet       Date:  2009-09-22       Impact factor: 2.797

4.  Upregulation of Nicotinic Acetylcholine Receptor alph4+beta2 through a Ligand-Independent PI3Kbeta Mechanism That Is Enhanced by TNFalpha and the Jak2/p38Mapk Pathways.

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  4 in total

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