Transcriptomics Analysis of Circular RNAs Differentially Expressed in Apoptotic HeLa Cells
Apoptosis is a form of regulated cell death that plays a critical role in survival and developmental homeostasis. There are numerous reports on regulation of apoptosis by protein-coding genes as well as small non-coding RNAs, such as microRNAs. However, there is no comprehensive investigation of cir...
| Published in: | Frontiers in Genetics |
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| Main Authors: | , , |
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2019-03-01
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| Online Access: | https://www.frontiersin.org/article/10.3389/fgene.2019.00176/full |
| _version_ | 1857114926987870208 |
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| author | Bilge Yaylak Ipek Erdogan Bunyamin Akgul |
| author_facet | Bilge Yaylak Ipek Erdogan Bunyamin Akgul |
| author_sort | Bilge Yaylak |
| collection | DOAJ |
| container_title | Frontiers in Genetics |
| description | Apoptosis is a form of regulated cell death that plays a critical role in survival and developmental homeostasis. There are numerous reports on regulation of apoptosis by protein-coding genes as well as small non-coding RNAs, such as microRNAs. However, there is no comprehensive investigation of circular RNAs (circRNA) that are differentially expressed under apoptotic conditions. We have performed a transcriptomics study in which we first triggered apoptosis in HeLa cells through treatment with four different agents, namely cisplatin, doxorubicin, TNF-α and anti-Fas mAb. Total RNAs isolated from control as well as treated cells were treated with RNAse R to eliminate the linear RNAs. The remaining RNAs were then subjected to deep-sequencing to identify differentially expressed circRNAs. Interestingly, some of the dys-regulated circRNAs were found to originate from protein-coding genes well-documented to regulate apoptosis. A number of candidate circRNAs were validated with qPCR with or without RNAse R treatment as well. We then took advantage of bioinformatics tools to investigate the coding potential of differentially expressed RNAs. Additionally, we examined the candidate circRNAs for the putative miRNA-binding sites and their putative target mRNAs. Our analyses point to a potential for circRNA-mediated sponging of miRNAs known to regulate apoptosis. In conclusion, this is the first transcriptomics study that provides a complete circRNA profile of apoptotic cells that might shed light onto the potential role of circRNAs in apoptosis. |
| format | Article |
| id | doaj-art-e6efea8a47fc4b51ac6cf3298e63b8bc |
| institution | Directory of Open Access Journals |
| issn | 1664-8021 |
| language | English |
| publishDate | 2019-03-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| spelling | doaj-art-e6efea8a47fc4b51ac6cf3298e63b8bc2025-08-19T19:11:11ZengFrontiers Media S.A.Frontiers in Genetics1664-80212019-03-011010.3389/fgene.2019.00176436737Transcriptomics Analysis of Circular RNAs Differentially Expressed in Apoptotic HeLa CellsBilge YaylakIpek ErdoganBunyamin AkgulApoptosis is a form of regulated cell death that plays a critical role in survival and developmental homeostasis. There are numerous reports on regulation of apoptosis by protein-coding genes as well as small non-coding RNAs, such as microRNAs. However, there is no comprehensive investigation of circular RNAs (circRNA) that are differentially expressed under apoptotic conditions. We have performed a transcriptomics study in which we first triggered apoptosis in HeLa cells through treatment with four different agents, namely cisplatin, doxorubicin, TNF-α and anti-Fas mAb. Total RNAs isolated from control as well as treated cells were treated with RNAse R to eliminate the linear RNAs. The remaining RNAs were then subjected to deep-sequencing to identify differentially expressed circRNAs. Interestingly, some of the dys-regulated circRNAs were found to originate from protein-coding genes well-documented to regulate apoptosis. A number of candidate circRNAs were validated with qPCR with or without RNAse R treatment as well. We then took advantage of bioinformatics tools to investigate the coding potential of differentially expressed RNAs. Additionally, we examined the candidate circRNAs for the putative miRNA-binding sites and their putative target mRNAs. Our analyses point to a potential for circRNA-mediated sponging of miRNAs known to regulate apoptosis. In conclusion, this is the first transcriptomics study that provides a complete circRNA profile of apoptotic cells that might shed light onto the potential role of circRNAs in apoptosis.https://www.frontiersin.org/article/10.3389/fgene.2019.00176/fullapoptosiscircular RNARNA-seqtranscriptomicsHeLa |
| spellingShingle | Bilge Yaylak Ipek Erdogan Bunyamin Akgul Transcriptomics Analysis of Circular RNAs Differentially Expressed in Apoptotic HeLa Cells apoptosis circular RNA RNA-seq transcriptomics HeLa |
| title | Transcriptomics Analysis of Circular RNAs Differentially Expressed in Apoptotic HeLa Cells |
| title_full | Transcriptomics Analysis of Circular RNAs Differentially Expressed in Apoptotic HeLa Cells |
| title_fullStr | Transcriptomics Analysis of Circular RNAs Differentially Expressed in Apoptotic HeLa Cells |
| title_full_unstemmed | Transcriptomics Analysis of Circular RNAs Differentially Expressed in Apoptotic HeLa Cells |
| title_short | Transcriptomics Analysis of Circular RNAs Differentially Expressed in Apoptotic HeLa Cells |
| title_sort | transcriptomics analysis of circular rnas differentially expressed in apoptotic hela cells |
| topic | apoptosis circular RNA RNA-seq transcriptomics HeLa |
| url | https://www.frontiersin.org/article/10.3389/fgene.2019.00176/full |
| work_keys_str_mv | AT bilgeyaylak transcriptomicsanalysisofcircularrnasdifferentiallyexpressedinapoptotichelacells AT ipekerdogan transcriptomicsanalysisofcircularrnasdifferentiallyexpressedinapoptotichelacells AT bunyaminakgul transcriptomicsanalysisofcircularrnasdifferentiallyexpressedinapoptotichelacells |
