Literature DB >> 15612037

Heterochromatin--many flavours, common themes.

Jeffrey M Craig1.   

Abstract

Heterochromatin remains condensed throughout the cell cycle, is generally transcriptionally inert and is built and maintained by groups of factors with each group member sharing a similar function. In mammals, these groups include sequence-specific transcriptional repressors, functional RNA and proteins involved in DNA and histone methylation. Heterochromatin is cemented together via interactions within and between each protein group and is maintained by the cell's replication machinery. It can be constitutive (permanent) or facultative (developmentally regulated) and be any size, from a gene promotor to a whole genome. By studying the formation of facultative heterochromatin, we have gained information about how heterochromatin is assembled. We have discovered that there are many different architectural plans for the building of heterochromatin, leading to a seemingly never-ending variety of heterochromatic loci, with each built according to a general rule. Copyright 2004 Wiley Periodicals, Inc.

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Year:  2005        PMID: 15612037     DOI: 10.1002/bies.20145

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  41 in total

Review 1.  Proteomic investigation of epigenetics in neuropsychiatric disorders: a missing link between genetics and behavior?

Authors:  Mariana D Plazas-Mayorca; Kent E Vrana
Journal:  J Proteome Res       Date:  2010-09-09       Impact factor: 4.466

2.  Efficient cell migration requires global chromatin condensation.

Authors:  Gabi Gerlitz; Michael Bustin
Journal:  J Cell Sci       Date:  2010-06-08       Impact factor: 5.285

Review 3.  Replication of heterochromatin: insights into mechanisms of epigenetic inheritance.

Authors:  Julie A Wallace; Terry L Orr-Weaver
Journal:  Chromosoma       Date:  2005-11-15       Impact factor: 4.316

4.  Histone lysine methylation patterns in human cell types are arranged in distinct three-dimensional nuclear zones.

Authors:  Roman Zinner; Heiner Albiez; Joachim Walter; Antoine H F M Peters; Thomas Cremer; Marion Cremer
Journal:  Histochem Cell Biol       Date:  2005-10-08       Impact factor: 4.304

Review 5.  Gene activation and deactivation related changes in the three-dimensional structure of chromatin.

Authors:  Eva Wegel; Peter Shaw
Journal:  Chromosoma       Date:  2005-11-12       Impact factor: 4.316

Review 6.  Kiss and break up--a safe passage to anaphase in mitosis and meiosis.

Authors:  Jeffrey M Craig; K H Andy Choo
Journal:  Chromosoma       Date:  2005-10-15       Impact factor: 4.316

7.  Transcriptionally active heterochromatin in rye B chromosomes.

Authors:  Mariana Carchilan; Margarida Delgado; Teresa Ribeiro; Pedro Costa-Nunes; Ana Caperta; Leonor Morais-Cecílio; R Neil Jones; Wanda Viegas; Andreas Houben
Journal:  Plant Cell       Date:  2007-06-22       Impact factor: 11.277

8.  B chromosomes of B. dichromosomatica show a reduced level of euchromatic histone H3 methylation marks.

Authors:  Sylvia Marschner; Katrin Kumke; Andreas Houben
Journal:  Chromosome Res       Date:  2007-02-05       Impact factor: 5.239

Review 9.  HIV-1 transcription and latency: an update.

Authors:  Carine Van Lint; Sophie Bouchat; Alessandro Marcello
Journal:  Retrovirology       Date:  2013-06-26       Impact factor: 4.602

10.  INCURVATA2 encodes the catalytic subunit of DNA Polymerase alpha and interacts with genes involved in chromatin-mediated cellular memory in Arabidopsis thaliana.

Authors:  José María Barrero; Rebeca González-Bayón; Juan Carlos del Pozo; María Rosa Ponce; José Luis Micol
Journal:  Plant Cell       Date:  2007-09-14       Impact factor: 11.277

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