Cargando…

Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects

Faithful chromosome segregation in all eukaryotes relies on centromeres, the chromosomal sites that recruit kinetochore proteins and mediate spindle attachment during cell division. The centromeric histone H3 variant, CenH3, is the defining chromatin component of centromeres in most eukaryotes, incl...

Descripción completa

Detalles Bibliográficos
Autores principales: Drinnenberg, Ines A, deYoung, Dakota, Henikoff, Steven, Malik, Harmit Singh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359364/
https://www.ncbi.nlm.nih.gov/pubmed/25247700
http://dx.doi.org/10.7554/eLife.03676
_version_ 1782361390331199488
author Drinnenberg, Ines A
deYoung, Dakota
Henikoff, Steven
Malik, Harmit Singh
author_facet Drinnenberg, Ines A
deYoung, Dakota
Henikoff, Steven
Malik, Harmit Singh
author_sort Drinnenberg, Ines A
collection PubMed
description Faithful chromosome segregation in all eukaryotes relies on centromeres, the chromosomal sites that recruit kinetochore proteins and mediate spindle attachment during cell division. The centromeric histone H3 variant, CenH3, is the defining chromatin component of centromeres in most eukaryotes, including animals, fungi, plants, and protists. In this study, using detailed genomic and transcriptome analyses, we show that CenH3 was lost independently in at least four lineages of insects. Each of these lineages represents an independent transition from monocentricity (centromeric determinants localized to a single chromosomal region) to holocentricity (centromeric determinants extended over the entire chromosomal length) as ancient as 300 million years ago. Holocentric insects therefore contain a CenH3-independent centromere, different from almost all the other eukaryotes. We propose that ancient transitions to holocentricity in insects obviated the need to maintain CenH3, which is otherwise essential in most eukaryotes, including other holocentrics. DOI: http://dx.doi.org/10.7554/eLife.03676.001
format Online
Article
Text
id pubmed-4359364
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-43593642015-03-16 Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects Drinnenberg, Ines A deYoung, Dakota Henikoff, Steven Malik, Harmit Singh eLife Genes and Chromosomes Faithful chromosome segregation in all eukaryotes relies on centromeres, the chromosomal sites that recruit kinetochore proteins and mediate spindle attachment during cell division. The centromeric histone H3 variant, CenH3, is the defining chromatin component of centromeres in most eukaryotes, including animals, fungi, plants, and protists. In this study, using detailed genomic and transcriptome analyses, we show that CenH3 was lost independently in at least four lineages of insects. Each of these lineages represents an independent transition from monocentricity (centromeric determinants localized to a single chromosomal region) to holocentricity (centromeric determinants extended over the entire chromosomal length) as ancient as 300 million years ago. Holocentric insects therefore contain a CenH3-independent centromere, different from almost all the other eukaryotes. We propose that ancient transitions to holocentricity in insects obviated the need to maintain CenH3, which is otherwise essential in most eukaryotes, including other holocentrics. DOI: http://dx.doi.org/10.7554/eLife.03676.001 eLife Sciences Publications, Ltd 2014-09-23 /pmc/articles/PMC4359364/ /pubmed/25247700 http://dx.doi.org/10.7554/eLife.03676 Text en © 2014, Drinnenberg et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Genes and Chromosomes
Drinnenberg, Ines A
deYoung, Dakota
Henikoff, Steven
Malik, Harmit Singh
Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects
title Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects
title_full Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects
title_fullStr Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects
title_full_unstemmed Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects
title_short Recurrent loss of CenH3 is associated with independent transitions to holocentricity in insects
title_sort recurrent loss of cenh3 is associated with independent transitions to holocentricity in insects
topic Genes and Chromosomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4359364/
https://www.ncbi.nlm.nih.gov/pubmed/25247700
http://dx.doi.org/10.7554/eLife.03676
work_keys_str_mv AT drinnenberginesa recurrentlossofcenh3isassociatedwithindependenttransitionstoholocentricityininsects
AT deyoungdakota recurrentlossofcenh3isassociatedwithindependenttransitionstoholocentricityininsects
AT henikoffsteven recurrentlossofcenh3isassociatedwithindependenttransitionstoholocentricityininsects
AT malikharmitsingh recurrentlossofcenh3isassociatedwithindependenttransitionstoholocentricityininsects