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Preliminary RNA-Seq Analysis of Long Non-Coding RNAs Expressed in Human Term Placenta
Development of particular structures and proper functioning of the placenta are under the influence of sophisticated pathways, controlled by the expression of substantial genes that are additionally regulated by long non-coding RNAs (lncRNAs). To date, the expression profile of lncRNA in human term...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073670/ https://www.ncbi.nlm.nih.gov/pubmed/29954144 http://dx.doi.org/10.3390/ijms19071894 |
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author | Majewska, Marta Lipka, Aleksandra Paukszto, Lukasz Jastrzebski, Jan Pawel Gowkielewicz, Marek Jozwik, Marcin Majewski, Mariusz Krzysztof |
author_facet | Majewska, Marta Lipka, Aleksandra Paukszto, Lukasz Jastrzebski, Jan Pawel Gowkielewicz, Marek Jozwik, Marcin Majewski, Mariusz Krzysztof |
author_sort | Majewska, Marta |
collection | PubMed |
description | Development of particular structures and proper functioning of the placenta are under the influence of sophisticated pathways, controlled by the expression of substantial genes that are additionally regulated by long non-coding RNAs (lncRNAs). To date, the expression profile of lncRNA in human term placenta has not been fully established. This study was conducted to characterize the lncRNA expression profile in human term placenta and to verify whether there are differences in the transcriptomic profile between the sex of the fetus and pregnancy multiplicity. RNA-Seq data were used to profile, quantify, and classify lncRNAs in human term placenta. The applied methodology enabled detection of the expression of 4463 isoforms from 2899 annotated lncRNA loci, plus 990 putative lncRNA transcripts from 607 intergenic regions. Those placentally expressed lncRNAs displayed features such as shorter transcript length, longer exon length, fewer exons, and lower expression levels compared to messenger RNAs (mRNAs). Among all placental transcripts, 175,268 were classified as mRNAs and 15,819 as lncRNAs, and 56,727 variants were discovered within unannotated regions. Five differentially expressed lncRNAs (HAND2-AS1, XIST, RP1-97J1.2, AC010084.1, TTTY15) were identified by a sex-bias comparison. Splicing events were detected within 37 genes and 4 lncRNA loci. Functional analysis of cis-related potential targets for lncRNAs identified 2021 enriched genes. It is presumed that the obtained data will expand the current knowledge of lncRNAs in placenta and human non-coding catalogs, making them more contemporary and specific. |
format | Online Article Text |
id | pubmed-6073670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60736702018-08-13 Preliminary RNA-Seq Analysis of Long Non-Coding RNAs Expressed in Human Term Placenta Majewska, Marta Lipka, Aleksandra Paukszto, Lukasz Jastrzebski, Jan Pawel Gowkielewicz, Marek Jozwik, Marcin Majewski, Mariusz Krzysztof Int J Mol Sci Article Development of particular structures and proper functioning of the placenta are under the influence of sophisticated pathways, controlled by the expression of substantial genes that are additionally regulated by long non-coding RNAs (lncRNAs). To date, the expression profile of lncRNA in human term placenta has not been fully established. This study was conducted to characterize the lncRNA expression profile in human term placenta and to verify whether there are differences in the transcriptomic profile between the sex of the fetus and pregnancy multiplicity. RNA-Seq data were used to profile, quantify, and classify lncRNAs in human term placenta. The applied methodology enabled detection of the expression of 4463 isoforms from 2899 annotated lncRNA loci, plus 990 putative lncRNA transcripts from 607 intergenic regions. Those placentally expressed lncRNAs displayed features such as shorter transcript length, longer exon length, fewer exons, and lower expression levels compared to messenger RNAs (mRNAs). Among all placental transcripts, 175,268 were classified as mRNAs and 15,819 as lncRNAs, and 56,727 variants were discovered within unannotated regions. Five differentially expressed lncRNAs (HAND2-AS1, XIST, RP1-97J1.2, AC010084.1, TTTY15) were identified by a sex-bias comparison. Splicing events were detected within 37 genes and 4 lncRNA loci. Functional analysis of cis-related potential targets for lncRNAs identified 2021 enriched genes. It is presumed that the obtained data will expand the current knowledge of lncRNAs in placenta and human non-coding catalogs, making them more contemporary and specific. MDPI 2018-06-27 /pmc/articles/PMC6073670/ /pubmed/29954144 http://dx.doi.org/10.3390/ijms19071894 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Majewska, Marta Lipka, Aleksandra Paukszto, Lukasz Jastrzebski, Jan Pawel Gowkielewicz, Marek Jozwik, Marcin Majewski, Mariusz Krzysztof Preliminary RNA-Seq Analysis of Long Non-Coding RNAs Expressed in Human Term Placenta |
title | Preliminary RNA-Seq Analysis of Long Non-Coding RNAs Expressed in Human Term Placenta |
title_full | Preliminary RNA-Seq Analysis of Long Non-Coding RNAs Expressed in Human Term Placenta |
title_fullStr | Preliminary RNA-Seq Analysis of Long Non-Coding RNAs Expressed in Human Term Placenta |
title_full_unstemmed | Preliminary RNA-Seq Analysis of Long Non-Coding RNAs Expressed in Human Term Placenta |
title_short | Preliminary RNA-Seq Analysis of Long Non-Coding RNAs Expressed in Human Term Placenta |
title_sort | preliminary rna-seq analysis of long non-coding rnas expressed in human term placenta |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6073670/ https://www.ncbi.nlm.nih.gov/pubmed/29954144 http://dx.doi.org/10.3390/ijms19071894 |
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