Linear mRNA amplification approach for RNAseq from limited amount of RNA

Autor(es):Mostrar menos -

Ferreira, Elisa Napolitano ^[1] ; Molina, Gustavo de Campos ^[1] ; Puga, Renato David ^[2] ; Nagai, Maria Aparecida ^[3] ; Froes Marques Campos, Antonio Hugo Jose ^[1] ; Guimaraes, Gustavo Cardoso ^[1] ; Nunes, Diana Noronha ^[1] ; Pasqualini, Renata ^{[4, 5]} ; Arap, Wadih ^{[4, 5]} ; Brentani, Helena ^[6] ; Dias-Neto, Emmanuel ^{[1, 7]} ; Brentani, Ricardo R. ^[1] ; Carraro, Dirce Maria ^{[7, 1]}

Afiliação do(s) autor(es)

^[1] AC Camargo Canc Ctr, Int Res Ctr, BR-01508010 Sao Paulo, SP - Brazil

^[2] Hosp Israelita Albert Einstein, BR-05652000 Sao Paulo, SP - Brazil

^[3] Univ Sao Paulo, Fac Med, Radiol & Oncol Dept, BR-01246000 Sao Paulo, SP - Brazil

^[4] Univ New Mexico, Sch Med, Dept Internal Med, Div Hematol Oncol, Albuquerque, NM 87131 - USA

^[5] Univ New Mexico, Sch Med, Dept Internal Med, Div Mol Med, Albuquerque, NM 87131 - USA

^[6] Univ Sao Paulo, Fac Med, Dept Psychiat, BR-05403010 Sao Paulo, SP - Brazil

^[7] Natl Inst Sci & Technol Oncogen, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: Gene; v. 564, n. 2, p. 220-227, JUN 15 2015.
• Citações Web of Science: 1

Resumo

Whole-transcriptome evaluation by next-generation sequencing (NGS) has been widely applied in the investigation of diverse transcriptional scenarios. In many clinical situations, including needle biopsy samples or laser microdissected cells, limited amounts of RNA are usually available for the assessment of the whole transcriptome. Here, we describe an mRNA amplification protocol based on in vitro T7 transcription for transcriptome evaluation by NGS. Initially, we performed RNAseq from two human mammary epithelial cell lines and evaluated several aspects of the transcriptomes generated by linear amplification of Poly (A) mRNA species, including transcript representation, variability and abundance. Our protocol showed to be efficient with respect to full-length transcript coverage and quantitative expression levels. We then evaluated the applicability of using this protocol in a more realistic research scenario, analyzing tumor tissue samples microdissected by laser capture. In order to increase the quantification power of the libraries only the 3' end of transcripts were sequenced. We found highly reproducible RNAseq data among amplified tumor samples, with a median Spearman's correlation of 80%, strongly suggesting that the amplification step and library protocol preparation lead to a consistent transcriptional profile. Altogether, we established a robust protocol for assessing the polyadenylated transcriptome derived from limited amounts of total RNA that is applicable to all NGS platforms. (C) 2015 Elsevier B.V. All rights reserved. (AU)

• Processo FAPESP: 13/23277-8 - Aspectos moleculares envolvidos no risco, desenvolvimento e progressão do carcinoma ductal de mama: busca de novos genes de susceptibilidade e investigação da progressão do carcinoma in situ e do papel da mutação em BRCA1 no tumor triplo negativo
• Beneficiário: Dirce Maria Carraro
• Linha de fomento: Auxílio à Pesquisa - Temático