Cyclic nucleotide gated channel genes (CNGCs) in Rosaceae: genome-wide annotation, evolution and the roles on Valsa canker resistance
Key message In Rosaceae , tandem duplication caused the drastic expansion of CNGC gene family Group I. The members MdCN11 and MdCN19 negatively regulate Valsa canker resistance. Apple ( Malus domestica ) and pear ( Pyrus bretschneideri and P. communis ) are important fruit crops in Rosaceae family b...
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Veröffentlicht in: | Plant cell reports 2021-12, Vol.40 (12), p.2369-2382 |
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Sprache: | eng |
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Zusammenfassung: | Key message
In
Rosaceae
, tandem duplication caused the drastic expansion of CNGC gene family Group I. The members
MdCN11
and
MdCN19
negatively regulate
Valsa
canker resistance.
Apple (
Malus domestica
) and pear (
Pyrus bretschneideri
and
P. communis
) are important fruit crops in
Rosaceae
family but are suffering from threats of
Valsa
canker. Cyclic nucleotide-gated ion channels (CNGCs) take crucial roles in plant immune responses. In the present study, a total of 355 CNGCs was identified from 8
Rosaceae
plants. Based on phylogenetic analysis, 540 CNGCs from 18 plants (8 in
Rosaceae
and 10 others) could be divided into four groups. Group I was greatly expanded in
Rosaceae
resulted from tandem duplications. A large number of
cis
-acting regulatory elements (
cis
-elements) responsive to signals from multiple stresses and hormones were identified in the promoter regions of CNGCs in
Malus spp.
and
Pyrus spp
. Expressions of most Group I members were obviously up-regulated in
Valsa
canker susceptible varieties but not in the resistant ones. Furthermore, overexpression of the
MdCN11
and
MdCN19
in both apple fruits and ‘Duli’ (
P. betulifolia
) suspension cells compromised
Valsa
canker resistance. Overexpression of
MdCN11
induced expression of hypersensitive response (HR)-related genes. In conclusion, tandem duplication resulted in a drastic expansion of CNGC Group I members in
Rosaceae
. Among these,
MdCN11
and
MdCN19
negatively regulate the
Valsa
canker resistance via inducting HR. |
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ISSN: | 0721-7714 1432-203X |
DOI: | 10.1007/s00299-021-02778-2 |