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Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions
Human nucleolar organizer regions (NORs), containing ribosomal gene (rDNA) arrays, are located on the p-arms of acrocentric chromosomes (HSA13–15, 21, and 22). Absence of these p-arms from genome references has hampered research on nucleolar formation. Previously, we assembled a distal junction (DJ)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942050/ https://www.ncbi.nlm.nih.gov/pubmed/31727772 http://dx.doi.org/10.1101/gad.331892.119 |
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author | van Sluis, Marjolein Gailín, Michael Ó McCarter, Joseph G.W. Mangan, Hazel Grob, Alice McStay, Brian |
author_facet | van Sluis, Marjolein Gailín, Michael Ó McCarter, Joseph G.W. Mangan, Hazel Grob, Alice McStay, Brian |
author_sort | van Sluis, Marjolein |
collection | PubMed |
description | Human nucleolar organizer regions (NORs), containing ribosomal gene (rDNA) arrays, are located on the p-arms of acrocentric chromosomes (HSA13–15, 21, and 22). Absence of these p-arms from genome references has hampered research on nucleolar formation. Previously, we assembled a distal junction (DJ) DNA sequence contig that abuts rDNA arrays on their telomeric side, revealing that it is shared among the acrocentrics and impacts nucleolar organization. To facilitate inclusion into genome references, we describe sequencing the DJ from all acrocentrics, including three versions of HSA21, ∼3 Mb of novel sequence. This was achieved by exploiting monochromosomal somatic cell hybrids containing single human acrocentric chromosomes with NORs that retain functional potential. Analyses revealed remarkable DJ sequence and functional conservation among human acrocentrics. Exploring chimpanzee acrocentrics, we show that “DJ-like” sequences and abutting rDNA arrays are inverted as a unit in comparison to humans. Thus, rDNA arrays and linked DJs represent a conserved functional locus. We provide direct evidence for exchanges between heterologous human acrocentric p-arms, and uncover extensive structural variation between chromosomes and among individuals. These findings lead us to revaluate the molecular definition of NORs, identify novel genomic structural variation, and provide a rationale for the distinctive chromosomal organization of NORs. |
format | Online Article Text |
id | pubmed-6942050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-69420502020-01-16 Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions van Sluis, Marjolein Gailín, Michael Ó McCarter, Joseph G.W. Mangan, Hazel Grob, Alice McStay, Brian Genes Dev Research Paper Human nucleolar organizer regions (NORs), containing ribosomal gene (rDNA) arrays, are located on the p-arms of acrocentric chromosomes (HSA13–15, 21, and 22). Absence of these p-arms from genome references has hampered research on nucleolar formation. Previously, we assembled a distal junction (DJ) DNA sequence contig that abuts rDNA arrays on their telomeric side, revealing that it is shared among the acrocentrics and impacts nucleolar organization. To facilitate inclusion into genome references, we describe sequencing the DJ from all acrocentrics, including three versions of HSA21, ∼3 Mb of novel sequence. This was achieved by exploiting monochromosomal somatic cell hybrids containing single human acrocentric chromosomes with NORs that retain functional potential. Analyses revealed remarkable DJ sequence and functional conservation among human acrocentrics. Exploring chimpanzee acrocentrics, we show that “DJ-like” sequences and abutting rDNA arrays are inverted as a unit in comparison to humans. Thus, rDNA arrays and linked DJs represent a conserved functional locus. We provide direct evidence for exchanges between heterologous human acrocentric p-arms, and uncover extensive structural variation between chromosomes and among individuals. These findings lead us to revaluate the molecular definition of NORs, identify novel genomic structural variation, and provide a rationale for the distinctive chromosomal organization of NORs. Cold Spring Harbor Laboratory Press 2019-12-01 /pmc/articles/PMC6942050/ /pubmed/31727772 http://dx.doi.org/10.1101/gad.331892.119 Text en © 2019 van Sluis; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by/4.0/ This article, published in Genes & Development, is available under a Creative Commons License (Attribution 4.0 International), as described at http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Paper van Sluis, Marjolein Gailín, Michael Ó McCarter, Joseph G.W. Mangan, Hazel Grob, Alice McStay, Brian Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions |
title | Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions |
title_full | Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions |
title_fullStr | Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions |
title_full_unstemmed | Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions |
title_short | Human NORs, comprising rDNA arrays and functionally conserved distal elements, are located within dynamic chromosomal regions |
title_sort | human nors, comprising rdna arrays and functionally conserved distal elements, are located within dynamic chromosomal regions |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942050/ https://www.ncbi.nlm.nih.gov/pubmed/31727772 http://dx.doi.org/10.1101/gad.331892.119 |
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