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Non-coding RNA derived from a conservative subtelomeric tandem repeat in chicken and Japanese quail somatic cells

BACKGROUND: Subtelomeres are located close to the ends of chromosomes and organized by tandemly repetitive sequences, duplicated copies of genes, pseudogenes and retrotransposons. Transcriptional activity of tandemly organized DNA at terminal chromosomal regions and the distribution of subtelomere-d...

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Autores principales: Trofimova, Irina, Popova, Darya, Vasilevskaya, Elena, Krasikova, Alla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301066/
https://www.ncbi.nlm.nih.gov/pubmed/25610495
http://dx.doi.org/10.1186/s13039-014-0102-7
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author Trofimova, Irina
Popova, Darya
Vasilevskaya, Elena
Krasikova, Alla
author_facet Trofimova, Irina
Popova, Darya
Vasilevskaya, Elena
Krasikova, Alla
author_sort Trofimova, Irina
collection PubMed
description BACKGROUND: Subtelomeres are located close to the ends of chromosomes and organized by tandemly repetitive sequences, duplicated copies of genes, pseudogenes and retrotransposons. Transcriptional activity of tandemly organized DNA at terminal chromosomal regions and the distribution of subtelomere-derived non-coding RNAs are poorly investigated. Here we aimed to analyze transcriptional activity of subtelomeric tandem repeat in somatic tissues and cultured cells of birds. We focused on tissue-specific differences of subtelomeric repeats transcription, structure of the resulting transcripts and the behavior of subtelomere-derived RNA during mitosis. RESULTS: Transcriptional activity of short subtelomeric PO41 (“pattern of 41 bp”) tandem repeat in the somatic and cultured cells of chicken (Gallus gallus domesticus) and Japanese quail (Coturnix coturnix japonica) was examined using RNA fluorescence in situ hybridization approach. We discovered transcripts from both strands of the PO41 repeat in chicken MDCC-MSB1 cells as well as in chicken and Japanese quail somatic tissues, such as tissues of cerebellum, telencephalon, muscles, oviduct, small and large intestine. Normal somatic and transformed cells demonstrate similar distribution of PO41 repeat transcripts in interphase nuclei. We revealed one or two major foci of PO41 repeat transcripts associated with RNA polymerase II, representing nascent RNA, and dispersed PO41 repeat transcripts localized in euchromatin or interchromatin space, representing released RNA. During mitosis PO41 non-coding RNA distribute between condensed chromosomes till anaphase, when they concentrate at the cleavage plane. At telophase, clusters of PO41 RNA surround terminal regions of chromosomes. Treatments with RNases of different substrate specificity indicate that PO41 repeat transcripts are single-stranded RNAs with short double-stranded regions due to appearance of inverted repeats. CONCLUSION: Transcription of a subtelomeric tandem repeat in avian somatic cells is reported here for the first time. PO41 repeat transcription is conserved among Galliformes and has similar pattern in somatic tissues. We demonstrated redistribution of non-coding PO41 RNA occurring during the cell cycle. Potential regulatory role of the PO41 repeat transcripts in RNA-dependent process of subtelomere heterochromatin maintenance is discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13039-014-0102-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-43010662015-01-22 Non-coding RNA derived from a conservative subtelomeric tandem repeat in chicken and Japanese quail somatic cells Trofimova, Irina Popova, Darya Vasilevskaya, Elena Krasikova, Alla Mol Cytogenet Research BACKGROUND: Subtelomeres are located close to the ends of chromosomes and organized by tandemly repetitive sequences, duplicated copies of genes, pseudogenes and retrotransposons. Transcriptional activity of tandemly organized DNA at terminal chromosomal regions and the distribution of subtelomere-derived non-coding RNAs are poorly investigated. Here we aimed to analyze transcriptional activity of subtelomeric tandem repeat in somatic tissues and cultured cells of birds. We focused on tissue-specific differences of subtelomeric repeats transcription, structure of the resulting transcripts and the behavior of subtelomere-derived RNA during mitosis. RESULTS: Transcriptional activity of short subtelomeric PO41 (“pattern of 41 bp”) tandem repeat in the somatic and cultured cells of chicken (Gallus gallus domesticus) and Japanese quail (Coturnix coturnix japonica) was examined using RNA fluorescence in situ hybridization approach. We discovered transcripts from both strands of the PO41 repeat in chicken MDCC-MSB1 cells as well as in chicken and Japanese quail somatic tissues, such as tissues of cerebellum, telencephalon, muscles, oviduct, small and large intestine. Normal somatic and transformed cells demonstrate similar distribution of PO41 repeat transcripts in interphase nuclei. We revealed one or two major foci of PO41 repeat transcripts associated with RNA polymerase II, representing nascent RNA, and dispersed PO41 repeat transcripts localized in euchromatin or interchromatin space, representing released RNA. During mitosis PO41 non-coding RNA distribute between condensed chromosomes till anaphase, when they concentrate at the cleavage plane. At telophase, clusters of PO41 RNA surround terminal regions of chromosomes. Treatments with RNases of different substrate specificity indicate that PO41 repeat transcripts are single-stranded RNAs with short double-stranded regions due to appearance of inverted repeats. CONCLUSION: Transcription of a subtelomeric tandem repeat in avian somatic cells is reported here for the first time. PO41 repeat transcription is conserved among Galliformes and has similar pattern in somatic tissues. We demonstrated redistribution of non-coding PO41 RNA occurring during the cell cycle. Potential regulatory role of the PO41 repeat transcripts in RNA-dependent process of subtelomere heterochromatin maintenance is discussed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13039-014-0102-7) contains supplementary material, which is available to authorized users. BioMed Central 2014-12-23 /pmc/articles/PMC4301066/ /pubmed/25610495 http://dx.doi.org/10.1186/s13039-014-0102-7 Text en © Trofimova et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Trofimova, Irina
Popova, Darya
Vasilevskaya, Elena
Krasikova, Alla
Non-coding RNA derived from a conservative subtelomeric tandem repeat in chicken and Japanese quail somatic cells
title Non-coding RNA derived from a conservative subtelomeric tandem repeat in chicken and Japanese quail somatic cells
title_full Non-coding RNA derived from a conservative subtelomeric tandem repeat in chicken and Japanese quail somatic cells
title_fullStr Non-coding RNA derived from a conservative subtelomeric tandem repeat in chicken and Japanese quail somatic cells
title_full_unstemmed Non-coding RNA derived from a conservative subtelomeric tandem repeat in chicken and Japanese quail somatic cells
title_short Non-coding RNA derived from a conservative subtelomeric tandem repeat in chicken and Japanese quail somatic cells
title_sort non-coding rna derived from a conservative subtelomeric tandem repeat in chicken and japanese quail somatic cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4301066/
https://www.ncbi.nlm.nih.gov/pubmed/25610495
http://dx.doi.org/10.1186/s13039-014-0102-7
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