4.7 Article

In planta transcriptome analysis reveals tissue-specific expression of pathogenicity genes and microRNAs during rice-Magnaporthe interactions

Journal

GENOMICS
Volume 113, Issue 1, Pages 265-275

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ygeno.2020.12.018

Keywords

Neck blast; Leaf blast; Strand-specific RNA-sequencing; SmallRNAs

Funding

  1. Department of Biotechnology, Government of India
  2. Monsanto's Beachell-Borlaug International Fellowship Program (MBBISP)

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Transcriptional re-programming occurs in both host and pathogen during leaf and neck infection, resulting in tissue-specific and infection-specific gene expression patterns. Different sets of genes are uniquely expressed in leaf and neck tissues, with certain genes being up-regulated during infection in each tissue. MicroRNA sequencing reveals differential expression of microRNAs targeting specific transcripts in response to infection, providing insights into the dual-epidemics of blast disease.
Transcriptional re-programming in host and pathogen upon leaf and neck infection is an evolving area of research for the rice blast community. Analysis of in planta rice transcriptome in leaf and neck tissues revealed tissue-specific and infection-specific expression of rice and Magnaporthe oryzae genes in host and pathogen. The glycosyl hydrolase, isocitrate lyase, cupin domain containing protein, TF2, CMPG1, CHIT17 and OsCML14 genes were uniquely expressed in leaf infection. Genes like cytochrome P450, inhibitor I family protein, GSTU6, abscisic stress ripening, and cupin domain containing protein were up-regulated during neck infection. In our microRNA sequencing study, Osa-miR166n-3p was highly expressed in upon Magnaporthe leaf infection, whereas osa-miR1661-3p, osa-miR166n-3p and osa-miR159b were overexpressed in neck infection. Here we report several transcripts being targeted by up and down regulated microRNAs during infection. The putative genes expressed upon infection in leaf and neck could be used in understanding the dual-epidemics of blast disease.

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