Changes of cytosine methylation induced by wide hybridization and allopolyploidy in Cucumis

Genome ◽  
2008 ◽  
Vol 51 (10) ◽  
pp. 789-799 ◽  
Author(s):  
Longzheng Chen ◽  
Jinfeng Chen

We previously demonstrated that allopolyploidization could induce phenotypic variations and genome changes in a newly synthesized allotetraploid in Cucumis . To explore the molecular involvement of epigenetic phenomena, we investigated cytosine methylation in Cucumis by using methylation-sensitive amplified polymorphism (MSAP). Results revealed a twofold difference in the level of cytosine methylation between the reciprocal F1 hybrids and the allotetraploid. Analysis of the methylation pattern indicated that methylation changed at 2.0% to 6.4% of total sites in both the F1 hybrids and the allotetraploid compared with their corresponding parents. Furthermore, 68.2% to 80.0% of the changed sites showed an increase in cytosine methylation and a majority of the methylated sites were from the maternal parent. Observations in different generations of the allotetraploid found that the extent of change in cytosine methylation pattern between the S1 and S2 was significantly higher than that between the S2 and S3, suggesting stability in advanced generations. Analysis of 7 altered sequences indicated their similarity to known functional genes or genes involved in regulating gene expression. Reverse transcription – polymerase chain reaction analysis suggested that at least two of the methylation changes might be related to gene expression changes, which further supports the hypothesis that DNA methylation plays a significant role in allopolyploidization.

2004 ◽  
Vol 22 (4) ◽  
pp. 325-337 ◽  
Author(s):  
Hayati M. Iskandar ◽  
Robert S. Simpson ◽  
Rosanne E. Casu ◽  
Graham D. Bonnett ◽  
Donald J. Maclean ◽  
...  

2002 ◽  
Vol 49 (2) ◽  
pp. 147-156 ◽  
Author(s):  
Charles E. Shelburne ◽  
Raymond M. Gleason ◽  
Gregory R. Germaine ◽  
Larry F. Wolff ◽  
Brian H. Mullally ◽  
...  

2021 ◽  
Vol 3 (6) ◽  
pp. 44-50
Author(s):  
Javed Akram ◽  
Akram Tariq ◽  
Gibran Ali ◽  
Fridoon Jawad Ahmed ◽  
Syeda Saba Aslam

The endemic Vitamin D deficiency in Pakistan and the current COVID-19 epidemic have converged into a double whammy scenario in Pakistan [1]. Nutritional epigenomic studies have highlighted Vitamin D as a master Vitamin influencing various genomic expressions through its active metabolite 1α,25-dihydroxyvitamin D3 [2]. The objective of this study was to evaluate the measurable impact of adjuvant Cholecalciferol therapy in the Cytokine gene expression of COVID-19 patients by quantitative Real-Time Polymerase Chain Reaction analysis. The trial was a randomized control prospective open label interventional trial done on moderate to severe COVID-19 patients with deranged inflammatory and coagulation biomarkers. SunnyD STAT (Vitamin D3 200000 IU) softgels were given at Day 1, Day 3 and Day 5 of the treatment. Optimized quantitative Real-Time Polymerase Chain Reaction analysis showed decreased genetic expressions of Interleukin 6 (IL-6), Interleukin 2RA (IL-2RA) and Tumor Necrosis Factor (TNF-a) in the interventional group against the age and co-morbidities matched controls, providing molecular and genetic level evidence for the purported mechanism of amelioration of Cytokines induced pathogenic inflammation. However, inherent limitations of the design restrict the generalizability of the results and warrants caution for extrapolation. We recommend randomized placebo-controlled trials with larger sampling and genome wide profiling to infer more definite interpretations.


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