Arabidopsis thaliana
|
FWA
|
Late flowering |
Hypomethylation in the promoter region leading to higher expression |
Soppe et al., 2000
|
DWF4
|
Lack of elongation in shoots and petioles |
Insertion of CACTA family transposon that is activated by hypomethylation |
Miura et al., 2001
|
BNS
|
Short, compact inflorescence, reduced plant height |
Hypermethylation in the entire gene |
Saze and Kakutani, 2007
|
FASCIATA1
|
Abnormal flower development |
Insertion of gypsy class retrotransposon that is activated by hypomethylation |
Tsukahara et al., 2009
|
QTLs |
Enhanced growth |
De novo epigenetic variation resulting from the use of MSH1 silencing line |
Virdi et al., 2015
|
QTLs |
Flowering time, plant height, fruit number, biomass, root:shoot ratio |
Variation of DNA methylation resulting from the use of epigenetic inbred lines |
Johannes et al., 2009; Reinders et al., 2009; |
Canola
|
QTLs |
Variation of energy use efficiency (EUE) |
Epigenetic variation within the population |
Hauben et al., 2009
|
Cotton
|
COL2D |
Photoperiodicity |
Hypomethylation on the 5’ region |
Song et al., 2017
|
Linaria vulgaris
|
Lcyc
|
Radial symmetry (peloric) flower |
DNA methylated and transcriptionally silent |
Cubas et al., 1999
|
Maize
|
B1, R1, Pl1, P |
Anthocyanin pathway pigmentation of various shoot tissues |
Paramutation |
Hollick, 2017
|
low phytic acid 1 |
Reduced seed phytic acid, elevated seed inorganic P |
Paramutation |
Pilu et al., 2009
|
Melon
|
CmWIP1 |
Sex deteminaton |
Hypermethylation on promotor leading formation of female flower |
Martin et al., 2009
|
Oil palm
|
Karma |
Mantled trait from somaclonal variant |
Hypomethylation on karma |
Ong-Abdullah et al., 2015
|
Orange
|
ripening-related genes |
Ripening process |
Hypermethylation during fruit-repening |
Huang et al., 2019
|
Persimmon
|
MeGI |
Sex deteminaton |
Hypermethylation on the promoter region leading male flower, hypomethylation leads female flower |
Akagi et al., 2016
|
Rice
|
QTLs |
Energy use efficiency (EUE), enhanced seed yield |
Epigenetic variation within the population |
Schmidt et al., 2018
|
RIZBZ1, RPBF |
Aleurone layer formation |
Demethylation by OsROS1a during grain maturation |
Liu et al., 2018
|
D1 |
Dwarfing |
Hypermethylation and repressive histone mark on the promoter region |
Miura et al., 2009
|
OsFIE1 |
Dwarfing, flower developement |
Hypomethylation and H3K9me2 depleation on the 5’ region |
Zhang et al., 2012
|
RAV6 |
Leaf angle |
Hypomethylation on the promoter region |
Zhang et al., 2015
|
OsAK1 |
Chlorophyll formation |
Hypermethylation on the promoter region |
Wei et al., 2017
|
OsSPL14 |
Grain yield |
Hypomethylation on upstream 2.6-kb region |
Miura et al., 2010
|
Sorghum
|
QTLs |
Grain yield, tiller number, plant height, flowering time |
De novo epigenetic variation resulting from the use of MSH1 silencing line |
Ketumile et al., 2022
|
Soybean
|
QTLs |
Reduced growth rate, male sterility, enhanced branching and altered leaf and floral morphology |
De novo epigenetic variation resulting from the use of MSH1 silencing line |
Raju et al., 2018
|
Strawberry
|
ripening-related genes |
Ripening process |
Demethylation during fruit-repening |
Cheng et al., 2018
|
Tomato
|
SLTAB2
|
SULFUREA
|
Paramutation |
Gouil et al., 2016
|
QTLs |
Leaf morphology, variegation, dwarfing, male sterility, flower development, and flower timing |
De novo epigenetic variation resulting from the use of MSH1 silencing line |
Yang et al., 2015
|
LeSPL-CNR
|
Abnormal ripening, colorless fruit |
Silencing of expression by increased DNA methylaiton in the promoter region |
Manning et al., 2006
|
CNR, VTE3
|
Ripening process |
Demethylation by SlDML2 during fruit-repening |
Liu et al., 2018
|