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Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome

In human chromosomes, centromeric regions comprise megabase-size arrays of 171 bp alpha-satellite DNA monomers. The large distances spanned by these arrays preclude their replication from external sites and imply that the repetitive monomers contain replication origins. However, replication within t...

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Autores principales: Erliandri, Indri, Fu, Haiqing, Nakano, Megumi, Kim, Jung-Hyun, Miga, Karen H., Liskovykh, Mikhail, Earnshaw, William C., Masumoto, Hiroshi, Kouprina, Natalay, Aladjem, Mirit I., Larionov, Vladimir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191410/
https://www.ncbi.nlm.nih.gov/pubmed/25228468
http://dx.doi.org/10.1093/nar/gku835
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author Erliandri, Indri
Fu, Haiqing
Nakano, Megumi
Kim, Jung-Hyun
Miga, Karen H.
Liskovykh, Mikhail
Earnshaw, William C.
Masumoto, Hiroshi
Kouprina, Natalay
Aladjem, Mirit I.
Larionov, Vladimir
author_facet Erliandri, Indri
Fu, Haiqing
Nakano, Megumi
Kim, Jung-Hyun
Miga, Karen H.
Liskovykh, Mikhail
Earnshaw, William C.
Masumoto, Hiroshi
Kouprina, Natalay
Aladjem, Mirit I.
Larionov, Vladimir
author_sort Erliandri, Indri
collection PubMed
description In human chromosomes, centromeric regions comprise megabase-size arrays of 171 bp alpha-satellite DNA monomers. The large distances spanned by these arrays preclude their replication from external sites and imply that the repetitive monomers contain replication origins. However, replication within these arrays has not previously been profiled and the role of alpha-satellite DNA in initiation of DNA replication has not yet been demonstrated. Here, replication of alpha-satellite DNA in endogenous human centromeric regions and in de novo formed Human Artificial Chromosome (HAC) was analyzed. We showed that alpha-satellite monomers could function as origins of DNA replication and that replication of alphoid arrays organized into centrochromatin occurred earlier than those organized into heterochromatin. The distribution of inter-origin distances within centromeric alphoid arrays was comparable to the distribution of inter-origin distances on randomly selected non-centromeric chromosomal regions. Depletion of CENP-B, a kinetochore protein that binds directly to a 17 bp CENP-B box motif common to alpha-satellite DNA, resulted in enrichment of alpha-satellite sequences for proteins of the ORC complex, suggesting that CENP-B may have a role in regulating the replication of centromeric regions. Mapping of replication initiation sites in the HAC revealed that replication preferentially initiated in transcriptionally active regions.
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spelling pubmed-41914102015-04-02 Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome Erliandri, Indri Fu, Haiqing Nakano, Megumi Kim, Jung-Hyun Miga, Karen H. Liskovykh, Mikhail Earnshaw, William C. Masumoto, Hiroshi Kouprina, Natalay Aladjem, Mirit I. Larionov, Vladimir Nucleic Acids Res Genome Integrity, Repair and Replication In human chromosomes, centromeric regions comprise megabase-size arrays of 171 bp alpha-satellite DNA monomers. The large distances spanned by these arrays preclude their replication from external sites and imply that the repetitive monomers contain replication origins. However, replication within these arrays has not previously been profiled and the role of alpha-satellite DNA in initiation of DNA replication has not yet been demonstrated. Here, replication of alpha-satellite DNA in endogenous human centromeric regions and in de novo formed Human Artificial Chromosome (HAC) was analyzed. We showed that alpha-satellite monomers could function as origins of DNA replication and that replication of alphoid arrays organized into centrochromatin occurred earlier than those organized into heterochromatin. The distribution of inter-origin distances within centromeric alphoid arrays was comparable to the distribution of inter-origin distances on randomly selected non-centromeric chromosomal regions. Depletion of CENP-B, a kinetochore protein that binds directly to a 17 bp CENP-B box motif common to alpha-satellite DNA, resulted in enrichment of alpha-satellite sequences for proteins of the ORC complex, suggesting that CENP-B may have a role in regulating the replication of centromeric regions. Mapping of replication initiation sites in the HAC revealed that replication preferentially initiated in transcriptionally active regions. Oxford University Press 2014-10-13 2014-09-16 /pmc/articles/PMC4191410/ /pubmed/25228468 http://dx.doi.org/10.1093/nar/gku835 Text en Published by Oxford University Press on behalf of Nucleic Acids Research 2014. This work is written by (a) US Government employee(s) and is in the public domain in the US.
spellingShingle Genome Integrity, Repair and Replication
Erliandri, Indri
Fu, Haiqing
Nakano, Megumi
Kim, Jung-Hyun
Miga, Karen H.
Liskovykh, Mikhail
Earnshaw, William C.
Masumoto, Hiroshi
Kouprina, Natalay
Aladjem, Mirit I.
Larionov, Vladimir
Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome
title Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome
title_full Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome
title_fullStr Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome
title_full_unstemmed Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome
title_short Replication of alpha-satellite DNA arrays in endogenous human centromeric regions and in human artificial chromosome
title_sort replication of alpha-satellite dna arrays in endogenous human centromeric regions and in human artificial chromosome
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4191410/
https://www.ncbi.nlm.nih.gov/pubmed/25228468
http://dx.doi.org/10.1093/nar/gku835
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