Transcriptional patterns ofCoffea arabicaL. nitrate reductase, glutamine and asparagine synthetase genes are modulated under nitrogen suppression and coffee leaf rust
Author(s) -
Viviane Yumi Baba,
Masako Toma Braghini,
Tiago Benedito dos Santos,
Kênia Mara Baiocchi de Carvalho,
João Danillo Moura Soares,
Suzana Tiemi Ivamoto,
Mirian Perez Maluf,
Lílian Padilha,
Luzia Doretto Paccola-Meirelles,
Luiz Filipe Protásio Pereira,
Douglas Silva Domingues
Publication year - 2020
Publication title -
peerj
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.927
H-Index - 70
ISSN - 2167-8359
DOI - 10.7717/peerj.8320
Subject(s) - glutamine synthetase , biology , coffea arabica , asparagine synthetase , inoculation , nitrate reductase , gene , asparagine , enzyme , glutamine , horticulture , botany , biochemistry , amino acid
This study evaluated the transcriptional profile of genes related to nitrogen (N) assimilation in coffee plants susceptible and resistant to rust fungi under N sufficiency and N suppression. For this purpose, we inoculated young coffee leaves with Hemileia vastatrix uredospores and collected them at 0, 12, 24 and 48 hours post-inoculation (HPI) to evaluate the relative expressions of genes encoding cytosolic glutamine synthetase ( CaGS 1 ), plastid glutamine synthetase ( CaGS 2 ), nitrate reductase ( CaNR ), and asparagine synthetase ( CaAS ). The genes exhibited distinct patterns of transcriptional modulation for the different genotypes and N nutritional regimes. The resistant genotype (I59) presented high levels of transcription in response to pathogen inoculation for CaNR and CaGS 1 genes, evaluated under N sufficiency in the initial moments of infection (12 HPI). The gene CaGS 1 also showed a peak at 48 HPI. The susceptible genotype (CV99) showed increased transcript rates of CaNR at 12 and 24 HPI in response to rust inoculation. The transcriptional patterns observed for CV99, under N suppression, were high levels for CaAS and CaGS 2 at all post-inoculation times in response to coffee leaf rust disease. In addition, CaGS 1 was up-regulated at 48 HPI for CV99. Cultivar I59 showed high transcript levels at 12 HPI for CaAS and peaks at 24 and 48 HPI for CaGS 2 in inoculated samples. Consequently, total chlorophyl concentration was influenced by N suppression and by rust infection. Regarding enzyme activities in vitro for glutamine synthetase and CaNR , there was an increase in infected coffee leaves (I59) and under N sufficiency. Moreover, CV99 was modulated in both N nutritional regimes for GS activity in response to rust. Our results indicate that N transport genes trigger a differential modulation between genotypes through the action of rust disease.
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