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Strand-specific RNA-seq analyses of fruiting body development in Coprinopsis cinerea

  • Author(s): Muraguchi, H
  • Umezawa, K
  • Niikura, M
  • Yoshida, M
  • Kozaki, T
  • Ishii, K
  • Sakai, K
  • Shimizu, M
  • Nakahori, K
  • Sakamoto, Y
  • Choi, C
  • Ngan, CY
  • Lindquist, E
  • Lipzen, A
  • Tritt, A
  • Haridas, S
  • Barry, K
  • Grigoriev, IV
  • Pukkila, PJ
  • et al.
Abstract

© 2015 Muraguchi et al.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 credited. The basidiomycete fungus Coprinopsis cinerea is an important model system for multicellular development. Fruiting bodies of C. cinerea are typical mushrooms, which can be produced synchronously on defined media in the laboratory. To investigate the transcriptome in detail during fruiting body development, high-throughput sequencing (RNA-seq) was performed using cDNA libraries strand-specifically constructed from 13 points (stages/tissues) with two biological replicates. The reads were aligned to 14,245 predicted transcripts, and counted for forward and reverse transcripts. Differentially expressed genes (DEGs) between two adjacent points and between vegetative mycelium and each point were detected by Tag Count Comparison (TCC). To validate RNA-seq data, expression levels of selected genes were compared using RPKM values in RNA-seq data and qRT-PCR data, and DEGs detected in microarray data were examined in MA plots of RNA-seq data by TCC. We discuss events deduced from GO analysis of DEGs. In addition, we uncovered both transcription factor candidates and antisense transcripts that are likely to be involved in developmental regulation for fruiting.

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