Hormonal and epigenetic regulation during embryogenic tissue habituation in Cucurbita pepo L
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
26403461
DOI
10.1007/s00299-015-1869-7
PII: 10.1007/s00299-015-1869-7
Knihovny.cz E-resources
- Keywords
- ABA, CKs, DNA methylation, Habituation, IAA, Somatic embryogenesis,
- MeSH
- Azacitidine pharmacology MeSH
- Cucurbita drug effects embryology genetics MeSH
- Cytokinins metabolism MeSH
- Epigenesis, Genetic drug effects MeSH
- Herbicides pharmacology MeSH
- Enzyme Inhibitors pharmacology MeSH
- 2,4-Dichlorophenoxyacetic Acid pharmacology MeSH
- Abscisic Acid metabolism MeSH
- Indoleacetic Acids metabolism MeSH
- DNA Methylation drug effects MeSH
- Plant Growth Regulators metabolism MeSH
- Plant Somatic Embryogenesis Techniques MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Azacitidine MeSH
- Cytokinins MeSH
- Herbicides MeSH
- indoleacetic acid MeSH Browser
- Enzyme Inhibitors MeSH
- 2,4-Dichlorophenoxyacetic Acid MeSH
- Abscisic Acid MeSH
- Indoleacetic Acids MeSH
- Plant Growth Regulators MeSH
Habituated embryogenic line of pumpkin contained more CKs and IAA, but less ABA than the non-habituated line. Pronounced hypomethylation correlated with the absence of 2,4-D, addition of 5-azaC, and the process of habituation. A comparative analysis between habituated and non-habituated embryogenic cultures of pumpkin (Cucurbita pepo L.) in relation to endogenous phytohormones, global DNA methylation, and developmental and regeneration capacities of the cultures was conducted. The analysis revealed more cytokinins (CKs) and indole-3-acetic acid (IAA), but less abscisic acid (ABA) in the habituated HEC line than in the non-habituated DEC line. Ribosides and ribotides were the most abundant CK forms in both HEC and DEC lines (75.9 and 57.6 %, respectively). HEC contained more free-base CKs (5.8 vs. 3.2 %), whereas DEC contained considerably more O-glycosides (39.1 vs. 18.3 %). Although prevalence of IAA was common for both lines, relative ratio of CKs and ABA differed between DEC and HEC lines. ABA was prevailing over CKs in DEC, while CKs prevailed over ABA in HEC line. Taking into account the importance of ABA for embryo maturation, the reduced endogenous ABA content in HEC line might be the reason for a 5-fold reduction in regeneration capacity compared to DEC. Both habituated and non-habituated embryogenic lines were highly methylated in the presence of 2,4-dichlorophenoxyacetic acid (2,4-D). Pronounced hypomethylation correlated with the absence of 2,4-D, addition of 5-azacytidine (5-azaC), but also with the process of habituation. The habituated line was resistant to the effect of hypomethylation drug 5-azaC and remained highly methylated even after the addition of 5-azaC. Also, 5-azaC did not change the developmental pattern in the habituated line, indicating the existence of separate mechanisms by which 2,4-D influences global DNA methylation in comparison to habituation-related global DNA methylation.
Faculty of Science University of Zagreb Horvatovac 102a 10000 Zagreb Croatia
Institute Ruđer Bošković Bijenička cesta 54 10000 Zagreb Croatia
See more in PubMed
Theor Appl Genet. 1989 Mar;77(3):325-31 PubMed
Nucleic Acids Res. 1977;4(5):1257-65 PubMed
Dev Growth Differ. 2010 Aug;52(6):555-66 PubMed
Planta. 2006 Mar;223(4):637-45 PubMed
J Plant Physiol. 2004 Feb;161(2):229-36 PubMed
Trends Plant Sci. 2000 Dec;5(12):506-8 PubMed
Biochim Biophys Acta. 2011 Aug;1809(8):444-51 PubMed
Plant Physiol. 2006 Apr;140(4):1255-78 PubMed
Plant Physiol Biochem. 2005 Jul;43(7):681-91 PubMed
New Phytol. 2010 Jun;186(4):856-68 PubMed
Cancer Res. 1983 Feb;43(2):763-9 PubMed
Anal Biochem. 1964 Dec;9:431-42 PubMed
Nat Rev Genet. 2010 Mar;11(3):204-20 PubMed
Plant Cell. 2006 Apr;18(4):805-14 PubMed
Annu Rev Genet. 1989;23:395-408 PubMed
Plant Physiol. 2002 Aug;129(4):1807-19 PubMed
Plant Cell Rep. 2004 Sep;23(3):120-7 PubMed
Plant Cell Physiol. 2012 May;53(5):766-84 PubMed
Comp Biochem Physiol C Toxicol Pharmacol. 2014 Mar;160:54-9 PubMed
Development. 2003 Dec;130(25):6201-8 PubMed
Curr Top Dev Biol. 2004;60:55-89 PubMed
Nat Rev Genet. 2005 May;6(5):351-60 PubMed
Talanta. 2009 Dec 15;80(2):651-5 PubMed
Plant Cell Rep. 1991 Mar;9(11):623-6 PubMed
Plant Sci. 2000 Dec 7;160(1):15-26 PubMed
Talanta. 2009 Nov 15;80(1):390-9 PubMed
PLoS Genet. 2011 Aug;7(8):e1002243 PubMed
Genome. 1996 Apr;39(2):235-42 PubMed
Oncogene. 2002 Aug 12;21(35):5483-95 PubMed
J Chromatogr B Analyt Technol Biomed Life Sci. 2007 Mar 1;847(2):162-73 PubMed
Nat Rev Mol Cell Biol. 2011 Jul 22;12(8):483-92 PubMed
Phytochemistry. 2008 Aug;69(11):2214-24 PubMed
Int Rev Cytol. 2004;233:135-79 PubMed
Dev Genet. 1989;10(4):298-303 PubMed
Am J Bot. 2004 Nov;91(11):1743-56 PubMed