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Flavin-Containing Monooxygenases (FMO) Genes in Garlic Allium sativum L.: Genome-Wide Identification, Characterization, and Expression Analysis in Response to Fusarium proliferatum
In this study, 39 flavin-containing monooxygenase genes were identified in the genome of garlic ( Allium sativum L.). The distribution of AsFMOs into three phylogenetic clades associated with N-oxygenation (22 proteins), auxin biosynthesis (13 proteins), and S-oxygenation (4 proteins) has been shown...
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Published in: | Russian journal of genetics 2023-07, Vol.59 (7), p.654-668 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | In this study, 39 flavin-containing monooxygenase genes were identified in the genome of garlic (
Allium sativum
L.). The distribution of AsFMOs into three phylogenetic clades associated with N-oxygenation (22 proteins), auxin biosynthesis (13 proteins), and S-oxygenation (4 proteins) has been shown. FAD and NADPH binding, FMO-identifying, and FATGY motifs were found in the AsFMO sequences.
AsFMO
s transcripts were present in all garlic organs with a maximum in roots, leaves, peduncles, and air bulbs. In response to infection with the pathogenic fungus
Fusarium proliferatum
, differential expression of clade I genes (
AsFMO4
,
AsFMO11
,
AsFMO12
, and
AsFMO35
) was detected in the roots of cv. Sarmat and Strelets, contrasting in
Fusarium
rot resistance. At the same time, the expression response of the clade III
AsFMO18
gene involved in alliin biosynthesis was similar for both cultivars, regardless of their resistance/susceptibility to
Fusarium
. This suggests the redundancy of genes of clades I and III in plant responses to infection. The
AsFMO35
coding and regulatory sequences were analyzed in cv. Sarmat and Strelets. It was shown that the
AsFMO35
promoter differs by the presence of the ABA-associated
cis
-regulatory element ABRE in cv. Strelets susceptible to
Fusarium
rot. |
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ISSN: | 1022-7954 1608-3369 |
DOI: | 10.1134/S1022795423070025 |