Literature DB >> 26333994

The Histone Methyltransferase Gene Absent, Small, or Homeotic Discs-1 Like Is Required for Normal Hox Gene Expression and Fertility in Mice.

Michelle L Brinkmeier1, Krista A Geister2, Morgan Jones2, Meriam Waqas1, Ivan Maillard3, Sally A Camper4.   

Abstract

Chromatin remodeling influences gene expression in developing and adult organisms. Active and repressive marks of histone methylation dictate the embryonic expression boundaries of developmentally regulated genes, including the Hox gene cluster. Drosophila ash1 (absent, small or homeotic discs 1) gene encodes a histone methyltransferase essential for regulation of Hox gene expression that interacts genetically with other members of the trithorax group (TrxG). While mammalian members of the mixed lineage leukemia (Mll) family of TrxG genes have roles in regulation of Hox gene expression, little is known about the expression and function of the mammalian ortholog of the Drosophila ash1 gene, Ash1-like (Ash1l). Here we report the expression of mouse Ash1l gene in specific structures within various organs and provide evidence that reduced Ash1l expression has tissue-specific effects on mammalian development and adult homeostasis. Mutants exhibit partially penetrant postnatal lethality and failure to thrive. Surviving mutants have growth insufficiency, skeletal transformations, and infertility associated with developmental defects in both male and female reproductive organs. Specifically, expression of Hoxa11 and Hoxd10 are altered in the epididymis of Ash1l mutant males and Hoxa10 is reduced in the uterus of Ash1l mutant females. In summary, we show that the histone methyltransferase Ash1l is important for the development and function of several tissues and for proper expression of homeotic genes in mammals.
© 2015 by the Society for the Study of Reproduction, Inc.

Entities:  

Keywords:  Hoxa11; Hoxd10; abdominal fat; axial skeleton; epigenetic; infertility; reproduction

Mesh:

Substances:

Year:  2015        PMID: 26333994      PMCID: PMC4712006          DOI: 10.1095/biolreprod.115.131516

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  57 in total

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Review 3.  Histone-modifying enzymes: regulators of developmental decisions and drivers of human disease.

Authors:  Jill S Butler; Evangelia Koutelou; Andria C Schibler; Sharon Y R Dent
Journal:  Epigenomics       Date:  2012-04       Impact factor: 4.778

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Review 4.  Experimental Models to Study Autism Spectrum Disorders: hiPSCs, Rodents and Zebrafish.

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6.  ASH1L histone methyltransferase regulates the handoff between damage recognition factors in global-genome nucleotide excision repair.

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7.  Mrg15 stimulates Ash1 H3K36 methyltransferase activity and facilitates Ash1 Trithorax group protein function in Drosophila.

Authors:  Chang Huang; Fu Yang; Zhuqiang Zhang; Jing Zhang; Gaihong Cai; Lin Li; Yong Zheng; She Chen; Rongwen Xi; Bing Zhu
Journal:  Nat Commun       Date:  2017-11-21       Impact factor: 14.919

8.  The Trithorax protein Ash1L promotes myoblast fusion by activating Cdon expression.

Authors:  Ilaria Castiglioni; Roberta Caccia; Jose Manuel Garcia-Manteiga; Giulia Ferri; Giuseppina Caretti; Ivan Molineris; Kenichi Nishioka; Davide Gabellini
Journal:  Nat Commun       Date:  2018-11-28       Impact factor: 14.919

9.  A chromosome 1q22 microdeletion including ASH1L is associated with intellectual disability in a Chinese family.

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Journal:  Mol Cytogenet       Date:  2020-06-04       Impact factor: 2.009

10.  Mir142 loss unlocks IDH2R140-dependent leukemogenesis through antagonistic regulation of HOX genes.

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Journal:  Sci Rep       Date:  2020-11-10       Impact factor: 4.379

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