Discovery of CTCF-sensitive Cis-spliced fusion RNAs between adjacent genes in human prostate cells.
Genes or their encoded products are not expected to mingle with each other unless in some disease situations. In cancer, a frequent mechanism that can produce gene fusions is chromosomal rearrangement. However, recent discoveries of RNA trans-splicing and cis-splicing between adjacent genes (cis-SAG...
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doaj-777eaa1f471241bba46614f7af08b7722020-11-24T21:32:38ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042015-02-01112e100500110.1371/journal.pgen.1005001Discovery of CTCF-sensitive Cis-spliced fusion RNAs between adjacent genes in human prostate cells.Fujun QinZhenguo SongMihaela BabiceanuYansu SongLoryn FacemireRitambhara SinghMazhar AdliHui LiGenes or their encoded products are not expected to mingle with each other unless in some disease situations. In cancer, a frequent mechanism that can produce gene fusions is chromosomal rearrangement. However, recent discoveries of RNA trans-splicing and cis-splicing between adjacent genes (cis-SAGe) support for other mechanisms in generating fusion RNAs. In our transcriptome analyses of 28 prostate normal and cancer samples, 30% fusion RNAs on average are the transcripts that contain exons belonging to same-strand neighboring genes. These fusion RNAs may be the products of cis-SAGe, which was previously thought to be rare. To validate this finding and to better understand the phenomenon, we used LNCaP, a prostate cell line as a model, and identified 16 additional cis-SAGe events by silencing transcription factor CTCF and paired-end RNA sequencing. About half of the fusions are expressed at a significant level compared to their parental genes. Silencing one of the in-frame fusions resulted in reduced cell motility. Most out-of-frame fusions are likely to function as non-coding RNAs. The majority of the 16 fusions are also detected in other prostate cell lines, as well as in the 14 clinical prostate normal and cancer pairs. By studying the features associated with these fusions, we developed a set of rules: 1) the parental genes are same-strand-neighboring genes; 2) the distance between the genes is within 30kb; 3) the 5' genes are actively transcribing; and 4) the chimeras tend to have the second-to-last exon in the 5' genes joined to the second exon in the 3' genes. We then randomly selected 20 neighboring genes in the genome, and detected four fusion events using these rules in prostate cancer and non-cancerous cells. These results suggest that splicing between neighboring gene transcripts is a rather frequent phenomenon, and it is not a feature unique to cancer cells.http://europepmc.org/articles/PMC4450057?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Fujun Qin Zhenguo Song Mihaela Babiceanu Yansu Song Loryn Facemire Ritambhara Singh Mazhar Adli Hui Li |
spellingShingle |
Fujun Qin Zhenguo Song Mihaela Babiceanu Yansu Song Loryn Facemire Ritambhara Singh Mazhar Adli Hui Li Discovery of CTCF-sensitive Cis-spliced fusion RNAs between adjacent genes in human prostate cells. PLoS Genetics |
author_facet |
Fujun Qin Zhenguo Song Mihaela Babiceanu Yansu Song Loryn Facemire Ritambhara Singh Mazhar Adli Hui Li |
author_sort |
Fujun Qin |
title |
Discovery of CTCF-sensitive Cis-spliced fusion RNAs between adjacent genes in human prostate cells. |
title_short |
Discovery of CTCF-sensitive Cis-spliced fusion RNAs between adjacent genes in human prostate cells. |
title_full |
Discovery of CTCF-sensitive Cis-spliced fusion RNAs between adjacent genes in human prostate cells. |
title_fullStr |
Discovery of CTCF-sensitive Cis-spliced fusion RNAs between adjacent genes in human prostate cells. |
title_full_unstemmed |
Discovery of CTCF-sensitive Cis-spliced fusion RNAs between adjacent genes in human prostate cells. |
title_sort |
discovery of ctcf-sensitive cis-spliced fusion rnas between adjacent genes in human prostate cells. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Genetics |
issn |
1553-7390 1553-7404 |
publishDate |
2015-02-01 |
description |
Genes or their encoded products are not expected to mingle with each other unless in some disease situations. In cancer, a frequent mechanism that can produce gene fusions is chromosomal rearrangement. However, recent discoveries of RNA trans-splicing and cis-splicing between adjacent genes (cis-SAGe) support for other mechanisms in generating fusion RNAs. In our transcriptome analyses of 28 prostate normal and cancer samples, 30% fusion RNAs on average are the transcripts that contain exons belonging to same-strand neighboring genes. These fusion RNAs may be the products of cis-SAGe, which was previously thought to be rare. To validate this finding and to better understand the phenomenon, we used LNCaP, a prostate cell line as a model, and identified 16 additional cis-SAGe events by silencing transcription factor CTCF and paired-end RNA sequencing. About half of the fusions are expressed at a significant level compared to their parental genes. Silencing one of the in-frame fusions resulted in reduced cell motility. Most out-of-frame fusions are likely to function as non-coding RNAs. The majority of the 16 fusions are also detected in other prostate cell lines, as well as in the 14 clinical prostate normal and cancer pairs. By studying the features associated with these fusions, we developed a set of rules: 1) the parental genes are same-strand-neighboring genes; 2) the distance between the genes is within 30kb; 3) the 5' genes are actively transcribing; and 4) the chimeras tend to have the second-to-last exon in the 5' genes joined to the second exon in the 3' genes. We then randomly selected 20 neighboring genes in the genome, and detected four fusion events using these rules in prostate cancer and non-cancerous cells. These results suggest that splicing between neighboring gene transcripts is a rather frequent phenomenon, and it is not a feature unique to cancer cells. |
url |
http://europepmc.org/articles/PMC4450057?pdf=render |
work_keys_str_mv |
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