Mammalian Sex Hormones as Steroid-Structured Compounds in Wheat Seedling: Template of the Cytosine Methylation Alteration and Retrotransposon Polymorphisms with iPBS and CRED-iBPS Techniques

Author:

Demirel Fatih1ORCID,Türkoğlu Aras2ORCID,Haliloğlu Kamil3ORCID,Eren Barış1,Özkan Güller4,Uysal Pinar5,Pour-Aboughadareh Alireza6ORCID,Leśniewska-Bocianowska Agnieszka7ORCID,Jamshidi Bita8ORCID,Bocianowski Jan9ORCID

Affiliation:

1. Department of Agricultural Biotechnology, Faculty of Agriculture, Igdır University, Igdir 76000, Türkiye

2. Department of Field Crops, Faculty of Agriculture, Necmettin Erbakan University, Konya 42310, Türkiye

3. Department of Field Crops, Faculty of Agriculture, Ataturk University, Erzurum 25240, Türkiye

4. Department of Biology, Faculty of Science, Ankara University, Ankara 06100, Türkiye

5. Ministry of Food, Agriculture and Livestock, Eastern Anatolia Agricultural Research Institute, Erzurum 25090, Türkiye

6. Seed and Plant Improvement Institute, Agricultural Research, Education and Extension Organization (AREEO), Karaj P.O. Box 3158854119, Iran

7. Department of Pathophysiology of Ageing and Civilization Diseases, Poznan University of Medical Sciences, 61-848 Poznan, Poland

8. Department of Food Security and Public Health, Khabat Technical Institute, Erbil Polytechnic University, Erbil 44001, Iraq

9. Department of Mathematical and Statistical Methods, Poznan University of Life Sciences, 60-637 Poznan, Poland

Abstract

Phytohormones are chemical compounds found naturally in plants that have a significant effect on their growth and development. The increase in research on the occurrence of mammalian sex hormones (MSHs) in plants has prompted the need to investigate the functions performed by these hormones in plant biology. In the present study, we investigated the effects of MSHs on DNA damage and DNA methylation of wheat (Triticum aestivum L.) during the seedling growth stage, using the CRED-iPBS (coupled restriction enzyme digestion/inter primer binding site) assay and iPBS analysis to determine DNA methylation status. Exogenous treatment with four MSHs (17-β-estradiol, estrogen, progesterone, and testosterone) was carried out at four different concentrations (0, 0.05, 0.5, and 5 µM). The highest genomic template stability (GTS) value (80%) was observed for 5 µM 17-β-estradiol, 0.5 µM testosterone, and 0.05 µM estrogen, while the lowest value (70.7%) was observed for 5 µM progesterone and 0.5 µM estrogen. The results of the CRED-iPBS analysis conducted on MspI indicate that the 0.05 µM estrogen-treated group had the highest polymorphism value of 40%, while the 5 µM progesterone-treated group had the lowest value of 20%. For HpaII, treatment with 0.5 µM 17-β-estradiol had the highest polymorphism value of 33.3%, while the group treated with 0.05 µM 17-β-estradiol and 0.05 µM progesterone had the lowest value of 19.4%. In conclusion, MSH treatments altered the stability of the genomic template of wheat plants and affected the cytosine methylation status at the seedling growth stage. Upon comprehensive examination of the results, it was seen that the employed methodology successfully detected alterations in cytosine methylation of genomic DNA (gDNA), as well as changes in the pattern of genomic instability.

Publisher

MDPI AG

Subject

Fluid Flow and Transfer Processes,Computer Science Applications,Process Chemistry and Technology,General Engineering,Instrumentation,General Materials Science

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