Literature DB >> 34843088

Epigenetic control of centromere: what can we learn from neocentromere?

Taekyung Kim1.   

Abstract

BACKGROUND: The centromere is the special region on a chromosome, which serves as the site for assembly of kinetochore complex and is essential for maintaining genomic integrity. Neocentromeres are new centromeres that form on the non-centromeric regions of the chromosome when the natural centromere is disrupted or inactivated. Although neocentromeres lack the typical features found in centromeres, cells with neocentromeres divide normally during mitosis and meiosis. Neocentromeres not only arise naturally but their formation can also be induced experimentally. Therefore, neocentromeres are a great tool for studying functions and formation of centromeres.
OBJECTIVE: To study neocentromeres and use that knowledge to gain insights into the epigenetic regulation of canonical centromeres. DISCUSSION: Here, we review the characteristics of naturally occurring centromeres and neocentromeres and those of experimentally induced neocentromeres. We also discuss the mechanism of centromere formation and epigenetic regulation of centromere function, which we learned from studying the neocentromeres. Although neocentromeres lack main features of centromeres, such as presence of repetitive ⍺-satellite DNA and pericentric heterochromatin, they behave quite similar to the canonical centromere, indicating the epigenetic nature of the centromere. Still, further investigation will help to understand the formation and maintenance of the centromere, and the correlation to human diseases.
CONCLUSION: Neocentromeres helped us to understand the formation of canonical centromeres. Also, since neocentromeres are associated with certain cancer types, knowledge about them could be helpful to treat cancer.
© 2021. The Author(s) under exclusive licence to The Genetics Society of Korea.

Entities:  

Keywords:  CENP-A; Centromere; Chromosome; Epigenetics; Neocentromere

Mesh:

Year:  2021        PMID: 34843088     DOI: 10.1007/s13258-021-01193-x

Source DB:  PubMed          Journal:  Genes Genomics        ISSN: 1976-9571            Impact factor:   1.839


  76 in total

1.  A case of angioimmunoblastic T-cell non-Hodgkin lymphoma with a neocentric inv dup(1).

Authors:  Eric Blom; Fenna H Heyning; Wilma G M Kroes
Journal:  Cancer Genet Cytogenet       Date:  2010-10-01

2.  Altered dosage and mislocalization of histone H3 and Cse4p lead to chromosome loss in Saccharomyces cerevisiae.

Authors:  Wei-Chun Au; Matthew J Crisp; Steven Z DeLuca; Oliver J Rando; Munira A Basrai
Journal:  Genetics       Date:  2008-05-05       Impact factor: 4.562

3.  A paucity of heterochromatin at functional human neocentromeres.

Authors:  Alicia Alonso; Dan Hasson; Fanny Cheung; Peter E Warburton
Journal:  Epigenetics Chromatin       Date:  2010-03-08       Impact factor: 4.954

4.  Genomic microarray analysis reveals distinct locations for the CENP-A binding domains in three human chromosome 13q32 neocentromeres.

Authors:  Alicia Alonso; Radma Mahmood; Shulan Li; Fanny Cheung; Kinya Yoda; Peter E Warburton
Journal:  Hum Mol Genet       Date:  2003-08-19       Impact factor: 6.150

Review 5.  Neocentromeres: role in human disease, evolution, and centromere study.

Authors:  David J Amor; K H Andy Choo
Journal:  Am J Hum Genet       Date:  2002-08-26       Impact factor: 11.025

6.  Epigenetic engineering shows H3K4me2 is required for HJURP targeting and CENP-A assembly on a synthetic human kinetochore.

Authors:  Jan H Bergmann; Mariluz Gómez Rodríguez; Nuno M C Martins; Hiroshi Kimura; David A Kelly; Hiroshi Masumoto; Vladimir Larionov; Lars E T Jansen; William C Earnshaw
Journal:  EMBO J       Date:  2010-12-14       Impact factor: 11.598

7.  HJURP is a CENP-A chromatin assembly factor sufficient to form a functional de novo kinetochore.

Authors:  Meghan C Barnhart; P Henning J L Kuich; Madison E Stellfox; Jared A Ward; Emily A Bassett; Ben E Black; Daniel R Foltz
Journal:  J Cell Biol       Date:  2011-07-18       Impact factor: 10.539

8.  The past, present, and future of human centromere genomics.

Authors:  Megan E Aldrup-Macdonald; Beth A Sullivan
Journal:  Genes (Basel)       Date:  2014-01-24       Impact factor: 4.096

9.  CENP-A nucleosomes localize to transcription factor hotspots and subtelomeric sites in human cancer cells.

Authors:  Rajbir K Athwal; Marcin P Walkiewicz; Songjoon Baek; Song Fu; Minh Bui; Jordi Camps; Thomas Ried; Myong-Hee Sung; Yamini Dalal
Journal:  Epigenetics Chromatin       Date:  2015-01-13       Impact factor: 4.954

10.  Co-localization of CENP-C and CENP-H to discontinuous domains of CENP-A chromatin at human neocentromeres.

Authors:  Alicia Alonso; Björn Fritz; Dan Hasson; György Abrusan; Fanny Cheung; Kinya Yoda; Bernhard Radlwimmer; Andreas G Ladurner; Peter E Warburton
Journal:  Genome Biol       Date:  2007       Impact factor: 13.583

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