Literature DB >> 8288132

Acetylated histone H4 on the male X chromosome is associated with dosage compensation in Drosophila.

J R Bone1, J Lavender, R Richman, M J Palmer, B M Turner, M I Kuroda.   

Abstract

Dosage compensation in Drosophila occurs by an increase in transcription of genes on the X chromosome in males. This elevated expression requires the function of at least four loci, known collectively as the male-specific lethal (msl) genes. The proteins encoded by two of these genes, maleless (mle) and male-specific lethal-1 (msl-1), are found associated with the X chromosome in males, suggesting that they act as positive regulators of dosage compensation. A specific acetylated isoform of histone H4, H4Ac16, is also detected predominantly on the male X chromosome. We have found that MLE and MSL-1 bind to the X chromosome in an identical pattern and that the pattern of H4Ac16 on the X is largely coincident with that of MLE/MSL-1. We fail to detect H4Ac16 on the X chromosome in homozygous msl males, correlating with the lack of dosage compensation in these mutants. Conversely, in Sxl mutants, we detect H4Ac16 on the female X chromosomes, coincident with an inappropriate increase in X chromosome transcription. These data suggest that synthesis or localization of H4Ac16 is controlled by the dosage compensation regulatory hierarchy. Dosage compensation may involve H4Ac16 function, potentially through interaction with the product of the msl genes.

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Year:  1994        PMID: 8288132     DOI: 10.1101/gad.8.1.96

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  116 in total

1.  Critical role for the histone H4 N terminus in nucleosome remodeling by ISWI.

Authors:  C R Clapier; G Längst; D F Corona; P B Becker; K P Nightingale
Journal:  Mol Cell Biol       Date:  2001-02       Impact factor: 4.272

Review 2.  Above and within the genome: epigenetics past and present.

Authors:  F D Urnov; A P Wolffe
Journal:  J Mammary Gland Biol Neoplasia       Date:  2001-04       Impact factor: 2.673

3.  Specificity of the HP1 chromo domain for the methylated N-terminus of histone H3.

Authors:  S A Jacobs; S D Taverna; Y Zhang; S D Briggs; J Li; J C Eissenberg; C D Allis; S Khorasanizadeh
Journal:  EMBO J       Date:  2001-09-17       Impact factor: 11.598

Review 4.  The marks, mechanisms and memory of epigenetic states in mammals.

Authors:  V K Rakyan; J Preis; H D Morgan; E Whitelaw
Journal:  Biochem J       Date:  2001-05-15       Impact factor: 3.857

5.  Targeting the chromatin-remodeling MSL complex of Drosophila to its sites of action on the X chromosome requires both acetyl transferase and ATPase activities.

Authors:  W Gu; X Wei; A Pannuti; J C Lucchesi
Journal:  EMBO J       Date:  2000-10-02       Impact factor: 11.598

Review 6.  Acetylation of histones and transcription-related factors.

Authors:  D E Sterner; S L Berger
Journal:  Microbiol Mol Biol Rev       Date:  2000-06       Impact factor: 11.056

7.  Role of the male specific lethal (msl) genes in modifying the effects of sex chromosomal dosage in Drosophila.

Authors:  U Bhadra; M Pal-Bhadra; J A Birchler
Journal:  Genetics       Date:  1999-05       Impact factor: 4.562

8.  Functional integration of the histone acetyltransferase MOF into the dosage compensation complex.

Authors:  Violette Morales; Tobias Straub; Martin F Neumann; Gabrielle Mengus; Asifa Akhtar; Peter B Becker
Journal:  EMBO J       Date:  2004-05-13       Impact factor: 11.598

Review 9.  Nuclear organization and dosage compensation.

Authors:  Jennifer C Chow; Edith Heard
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-10-13       Impact factor: 10.005

10.  Carnitine suppression of position-effect variegation in Drosophila melanogaster.

Authors:  L Fanti; M Berloco; S Pimpinelli
Journal:  Mol Gen Genet       Date:  1994-09-28
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