Cargando…

Poly A- Transcripts Expressed in HeLa Cells

BACKGROUND: Transcripts expressed in eukaryotes are classified as poly A+ transcripts or poly A- transcripts based on the presence or absence of the 3′ poly A tail. Most transcripts identified so far are poly A+ transcripts, whereas the poly A- transcripts remain largely unknown. METHODOLOGY/PRINCIP...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Qingfa, Kim, Yeong C., Lu, Jian, Xuan, Zhenyu, Chen, Jun, Zheng, Yonglan, Zhou, Tom, Zhang, Michael Q., Wu, Chung-I, Wang, San Ming
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2481391/
https://www.ncbi.nlm.nih.gov/pubmed/18665230
http://dx.doi.org/10.1371/journal.pone.0002803
_version_ 1782157982008606720
author Wu, Qingfa
Kim, Yeong C.
Lu, Jian
Xuan, Zhenyu
Chen, Jun
Zheng, Yonglan
Zhou, Tom
Zhang, Michael Q.
Wu, Chung-I
Wang, San Ming
author_facet Wu, Qingfa
Kim, Yeong C.
Lu, Jian
Xuan, Zhenyu
Chen, Jun
Zheng, Yonglan
Zhou, Tom
Zhang, Michael Q.
Wu, Chung-I
Wang, San Ming
author_sort Wu, Qingfa
collection PubMed
description BACKGROUND: Transcripts expressed in eukaryotes are classified as poly A+ transcripts or poly A- transcripts based on the presence or absence of the 3′ poly A tail. Most transcripts identified so far are poly A+ transcripts, whereas the poly A- transcripts remain largely unknown. METHODOLOGY/PRINCIPAL FINDINGS: We developed the TRD (Total RNA Detection) system for transcript identification. The system detects the transcripts through the following steps: 1) depleting the abundant ribosomal and small-size transcripts; 2) synthesizing cDNA without regard to the status of the 3′ poly A tail; 3) applying the 454 sequencing technology for massive 3′ EST collection from the cDNA; and 4) determining the genome origins of the detected transcripts by mapping the sequences to the human genome reference sequences. Using this system, we characterized the cytoplasmic transcripts from HeLa cells. Of the 13,467 distinct 3′ ESTs analyzed, 24% are poly A-, 36% are poly A+, and 40% are bimorphic with poly A+ features but without the 3′ poly A tail. Most of the poly A- 3′ ESTs do not match known transcript sequences; they have a similar distribution pattern in the genome as the poly A+ and bimorphic 3′ ESTs, and their mapped intergenic regions are evolutionarily conserved. Experiments confirmed the authenticity of the detected poly A- transcripts. CONCLUSION/SIGNIFICANCE: Our study provides the first large-scale sequence evidence for the presence of poly A- transcripts in eukaryotes. The abundance of the poly A- transcripts highlights the need for comprehensive identification of these transcripts for decoding the transcriptome, annotating the genome and studying biological relevance of the poly A- transcripts.
format Text
id pubmed-2481391
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-24813912008-07-30 Poly A- Transcripts Expressed in HeLa Cells Wu, Qingfa Kim, Yeong C. Lu, Jian Xuan, Zhenyu Chen, Jun Zheng, Yonglan Zhou, Tom Zhang, Michael Q. Wu, Chung-I Wang, San Ming PLoS One Research Article BACKGROUND: Transcripts expressed in eukaryotes are classified as poly A+ transcripts or poly A- transcripts based on the presence or absence of the 3′ poly A tail. Most transcripts identified so far are poly A+ transcripts, whereas the poly A- transcripts remain largely unknown. METHODOLOGY/PRINCIPAL FINDINGS: We developed the TRD (Total RNA Detection) system for transcript identification. The system detects the transcripts through the following steps: 1) depleting the abundant ribosomal and small-size transcripts; 2) synthesizing cDNA without regard to the status of the 3′ poly A tail; 3) applying the 454 sequencing technology for massive 3′ EST collection from the cDNA; and 4) determining the genome origins of the detected transcripts by mapping the sequences to the human genome reference sequences. Using this system, we characterized the cytoplasmic transcripts from HeLa cells. Of the 13,467 distinct 3′ ESTs analyzed, 24% are poly A-, 36% are poly A+, and 40% are bimorphic with poly A+ features but without the 3′ poly A tail. Most of the poly A- 3′ ESTs do not match known transcript sequences; they have a similar distribution pattern in the genome as the poly A+ and bimorphic 3′ ESTs, and their mapped intergenic regions are evolutionarily conserved. Experiments confirmed the authenticity of the detected poly A- transcripts. CONCLUSION/SIGNIFICANCE: Our study provides the first large-scale sequence evidence for the presence of poly A- transcripts in eukaryotes. The abundance of the poly A- transcripts highlights the need for comprehensive identification of these transcripts for decoding the transcriptome, annotating the genome and studying biological relevance of the poly A- transcripts. Public Library of Science 2008-07-30 /pmc/articles/PMC2481391/ /pubmed/18665230 http://dx.doi.org/10.1371/journal.pone.0002803 Text en Wu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Wu, Qingfa
Kim, Yeong C.
Lu, Jian
Xuan, Zhenyu
Chen, Jun
Zheng, Yonglan
Zhou, Tom
Zhang, Michael Q.
Wu, Chung-I
Wang, San Ming
Poly A- Transcripts Expressed in HeLa Cells
title Poly A- Transcripts Expressed in HeLa Cells
title_full Poly A- Transcripts Expressed in HeLa Cells
title_fullStr Poly A- Transcripts Expressed in HeLa Cells
title_full_unstemmed Poly A- Transcripts Expressed in HeLa Cells
title_short Poly A- Transcripts Expressed in HeLa Cells
title_sort poly a- transcripts expressed in hela cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2481391/
https://www.ncbi.nlm.nih.gov/pubmed/18665230
http://dx.doi.org/10.1371/journal.pone.0002803
work_keys_str_mv AT wuqingfa polyatranscriptsexpressedinhelacells
AT kimyeongc polyatranscriptsexpressedinhelacells
AT lujian polyatranscriptsexpressedinhelacells
AT xuanzhenyu polyatranscriptsexpressedinhelacells
AT chenjun polyatranscriptsexpressedinhelacells
AT zhengyonglan polyatranscriptsexpressedinhelacells
AT zhoutom polyatranscriptsexpressedinhelacells
AT zhangmichaelq polyatranscriptsexpressedinhelacells
AT wuchungi polyatranscriptsexpressedinhelacells
AT wangsanming polyatranscriptsexpressedinhelacells