Cargando…
Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia
Mechanisms underlying severe male infertility are still largely elusive. However, recently, a single-cell transcription study by our group identified several differentially expressed coding genes in all the somatic cell types in testes of patients with idiopathic germ cell aplasia (iGCA). Here, we l...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486010/ https://www.ncbi.nlm.nih.gov/pubmed/36147743 http://dx.doi.org/10.3389/fcell.2022.952518 |
_version_ | 1784792183789846528 |
---|---|
author | Lavorgna, Giovanni Tascini, Anna Sofia Bertini, Alessandro Lanzaro, Francesco Montorsi, Francesco Alfano, Massimo Salonia, Andrea |
author_facet | Lavorgna, Giovanni Tascini, Anna Sofia Bertini, Alessandro Lanzaro, Francesco Montorsi, Francesco Alfano, Massimo Salonia, Andrea |
author_sort | Lavorgna, Giovanni |
collection | PubMed |
description | Mechanisms underlying severe male infertility are still largely elusive. However, recently, a single-cell transcription study by our group identified several differentially expressed coding genes in all the somatic cell types in testes of patients with idiopathic germ cell aplasia (iGCA). Here, we leverage this work by extending the analysis also to the non-coding portion of the genome. As a result, we found that 43 LncRNAs were differentially expressed in the somatic cells of these patients. Interestingly, a significant portion of the overexpressed LncRNAs was found to be a target of TAF9B, a transcription factor known to be involved in germ cell survival. Moreover, several overexpressed LncRNAs were also found to be activated in a mouse model of Sertoli cells treated with bisphenol A, a widespread environmental contaminant, long suspected to impair male fertility. Finally, a literature search for MEG3, a maternally imprinted LncRNA overexpressed as well in our patients, found it to be involved, among other things, in obesity and inflammation, known comorbidities of iGCA, ultimately suggesting that our findings deepen the understanding of the molecular insights coupled not only to the pathogenesis, but also to the clinical course of this class of patients. |
format | Online Article Text |
id | pubmed-9486010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94860102022-09-21 Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia Lavorgna, Giovanni Tascini, Anna Sofia Bertini, Alessandro Lanzaro, Francesco Montorsi, Francesco Alfano, Massimo Salonia, Andrea Front Cell Dev Biol Cell and Developmental Biology Mechanisms underlying severe male infertility are still largely elusive. However, recently, a single-cell transcription study by our group identified several differentially expressed coding genes in all the somatic cell types in testes of patients with idiopathic germ cell aplasia (iGCA). Here, we leverage this work by extending the analysis also to the non-coding portion of the genome. As a result, we found that 43 LncRNAs were differentially expressed in the somatic cells of these patients. Interestingly, a significant portion of the overexpressed LncRNAs was found to be a target of TAF9B, a transcription factor known to be involved in germ cell survival. Moreover, several overexpressed LncRNAs were also found to be activated in a mouse model of Sertoli cells treated with bisphenol A, a widespread environmental contaminant, long suspected to impair male fertility. Finally, a literature search for MEG3, a maternally imprinted LncRNA overexpressed as well in our patients, found it to be involved, among other things, in obesity and inflammation, known comorbidities of iGCA, ultimately suggesting that our findings deepen the understanding of the molecular insights coupled not only to the pathogenesis, but also to the clinical course of this class of patients. Frontiers Media S.A. 2022-09-06 /pmc/articles/PMC9486010/ /pubmed/36147743 http://dx.doi.org/10.3389/fcell.2022.952518 Text en Copyright © 2022 Lavorgna, Tascini, Bertini, Lanzaro, Montorsi, Alfano and Salonia. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Lavorgna, Giovanni Tascini, Anna Sofia Bertini, Alessandro Lanzaro, Francesco Montorsi, Francesco Alfano, Massimo Salonia, Andrea Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia |
title | Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia |
title_full | Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia |
title_fullStr | Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia |
title_full_unstemmed | Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia |
title_short | Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia |
title_sort | single-cell transcriptome profiling reveals several lncrnas differentially expressed in idiopathic germ cell aplasia |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486010/ https://www.ncbi.nlm.nih.gov/pubmed/36147743 http://dx.doi.org/10.3389/fcell.2022.952518 |
work_keys_str_mv | AT lavorgnagiovanni singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia AT tasciniannasofia singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia AT bertinialessandro singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia AT lanzarofrancesco singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia AT montorsifrancesco singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia AT alfanomassimo singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia AT saloniaandrea singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia |