Expression and DNA methylation of SERK, BBM, LEC2 and WUS genes in in vitro cultures of Boesenbergia rotunda (L.) Mansf
The process of somatic embryogenesis and plant regeneration involve changes in gene expression and have been associated with changes in DNA methylation. Here, we report the expression and DNA methylation patterns of SOMATIC EMBRYOGENESIS RECEPTOR - LIKE KINASE ( SERK ), BABY BOOM ( BBM ), LEAFY COTY...
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Veröffentlicht in: | Physiology and molecular biology of plants 2018-09, Vol.24 (5), p.741-751 |
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Zusammenfassung: | The process of somatic embryogenesis and plant regeneration involve changes in gene expression and have been associated with changes in DNA methylation. Here, we report the expression and DNA methylation patterns of
SOMATIC EMBRYOGENESIS RECEPTOR
-
LIKE KINASE
(
SERK
),
BABY BOOM
(
BBM
),
LEAFY COTYLEDON 2
(
LEC2
) and
WUSCHEL
(
WUS
) in meristematic block of newly emerged shoots from rhizome, embryogenic and non-embryogenic calli, prolonged cell suspension culture, ex vitro leaf, and in vitro leaf of regenerated plants of
Boesenbergia rotunda
. Among all seven samples, based on qRT-PCR, the highest level of expression of
SERK, BBM
and
LEC2
was in embryogenic callus, while
WUS
was most highly expressed in meristematic block tissue followed by embryogenic callus. Relatively lower expression was observed in cell suspension culture and watery callus for
SERK, LEC2
and
WUS
and in in vitro leaf for
BBM
. For gene specific methylation determined by bisulfite sequencing data, embryogenic callus samples had the lowest levels of DNA methylation at CG, CHG and CHH contexts of
SERK
,
LEC2
and
WUS
. We observed negative correlation between DNA methylation at the CG and CHG contexts and the expression levels of
SERK
,
BBM
,
LEC2
and
WUS
. Based on our results, we suggest that relatively higher expression and lower level of DNA methylation of
SERK, BBM
,
LEC2
and
WUS
are associated with somatic embryogenesis and plant regeneration in
B. rotunda
. |
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ISSN: | 0971-5894 0974-0430 |
DOI: | 10.1007/s12298-018-0566-8 |