Journals / Türkiye Tarımsal Araştırmalar Dergisi / 2017 / Cilt: 4 - Sayı: 1

Screening of Oryza sativa L. for Hpt Gene and Evaluation of Hpt Positive Samples Using Houba Retransposon-Based IRAP Markers

Pages
59–64
Publication Date
2017-02-28
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

This study is one of the first detailed experimental data of transgenic Oryza sativa L. samples in terms of retrotransposon-based variation.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Increasing world population needs to enhance agricultural production because of food starvation.
📊
Key Findings & Data:This produces spontaneous genetic changes with movement of transposable elements, and even increases variations.
💡
Conclusion & Impact:This study is one of the first detailed experimental data of transgenic Oryza sativa L. samples in terms of retrotransposon-based variation.
🔬Design:Research Article
📍Scope:6 samples
⚙️Variables:Genetically modified organism · Houba · IRAP

Abstract

Increasing world population needs to enhance agricultural production because of food starvation. Genetically modified organism (GMO) is a way to solve this problem. During gene transfers, DNA is inserted into a plant’s genome in a random way. This produces spontaneous genetic changes with movement of transposable elements, and even increases variations. Houba was described as one of the active retrotransposons in rice. The aim of this study was to screen rice samples collected from Turkey, and analyse Houba retrotransposon movements with IRAP technique in transgenic ones and their controls. For this purpose, 71 different rice seeds obtained from different regions of Turkey were used for GMO analysis. All samples were screened by real time PCR to test cauliflower mosaic virus (CaMV) 35S promoter (P-35S) regions, T-NOS (nopaline synthase terminator) regions, figwort mosaic virus (FMV) regions, bar, pat and Cry1ab/ac, and hpt (hygromycin resistance) genes. Hpt gene was identified in 6 samples as a result of real time PCR analysis. These 6 transgenic samples with their controls were used for IRAP-PCR analysis and 0-56% polymorphism ratios were observed in analysed samples. This study is one of the first detailed experimental data of transgenic Oryza sativa L. samples in terms of retrotransposon-based variation.

Özet

Increasing world population needs to enhance agricultural production because of food starvation. Genetically modified organism (GMO) is a way to solve this problem. During gene transfers, DNA is inserted into a plant’s genome in a random way. This produces spontaneous genetic changes with movement of transposable elements, and even increases variations. Houba was described as one of the active retrotransposons in rice. The aim of this study was to screen rice samples collected from Turkey, and analyse Houba retrotransposon movements with IRAP technique in transgenic ones and their controls. For this purpose, 71 different rice seeds obtained from different regions of Turkey were used for GMO analysis. All samples were screened by real time PCR to test cauliflower mosaic virus (CaMV) 35S promoter (P-35S) regions, T-NOS (nopaline synthase terminator) regions, figwort mosaic virus (FMV) regions, bar, pat and Cry1ab/ac, and hpt (hygromycin resistance) genes. Hpt gene was identified in 6 samples as a result of real time PCR analysis. These 6 transgenic samples with their controls were used for IRAP-PCR analysis and 0-56% polymorphism ratios were observed in analysed samples. This study is one of the first detailed experimental data of transgenic Oryza sativa L. samples in terms of retrotransposon-based variation.

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Cite This Article

YÜZBAŞIOĞLU, G., MARAKLI, S., GÖZÜKIRMIZI, N. (2017). Screening of Oryza sativa L. for Hpt Gene and Evaluation of Hpt Positive Samples Using Houba Retransposon-Based IRAP Markers. Türkiye Tarımsal Araştırmalar Dergisi, Cilt: 4 - Sayı: 1, 59–64. https://ajindex.com/articles/206565

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References (11)

  1. Anonymous, 2003. Regulation (EC) No 1830/2003 of the European Parliament and of the Council of 22 September 2003 concerning the traceability and labeling of genetically modified organisms and the traceability of food and feed products produced from genetically modified organisms and amending Directive2001/18/EC, Official Journal L, 268: 0024-0028. Anonymous, 2010a. Turkish Republic Biosafety Law: Law number 5977. Official Journal, 27533/Issue date: 26.03.2010. Anonymous, 2010b. Official Gazette of the Republic of Turkey. Number: 27533. Biosafety Law. Anonymous, 2011a. Official Gazette of the Republic of Turkey. Number: 27827, Biosecurity Committee Decisions, decision no.1, 2 and 3. Anonymous, 2011b. Official Gazette of the Republic of Turkey. Number: 28152, Biosecurity Committee Decisions, Decision No. 4-16.
  2. Baltes, N.J., Voytas, D.F., 2015. Enabling plant synthetic biology through genome engineering. Trends in Biotechnology, 33(2): 120-131.
  3. Barampuram, S., Zhang, Z.J., 2011. Recent advances in plant transformation. Plant Chromosome Engineering, pp. 1-35.
  4. Barroso, M.F., Freitas, M., Oliveira, M.B.P.P., De-Los-Santos-Alvarez, N., Lobo-Castanon, M.J., Deleure-Matos, C., 2015. 3D-nanostructured Au electrodes for the event-specific detection of MON810 transgenic maize. Talanta, 134: 158-164.
  5. Broeders, S.R.M., De Keersmaecker, S.C.J., Roosens, N.H., 2012. How to deal with the upcoming challenges in GMO detection in food and feed. Journal of Biomedicine and Biotechnology, 2012: 1-11.
  6. Cakmak, B., Marakli, S., Gozukirmizi, N., 2015. SIRE1 retrotransposons in barley (Hordeum vulgare L.). Russian Journal of Genetics, 51(7): 661-672.
  7. Cheema, H.M.N., Khan, A.A., Khan, M.I., Aslam, U., Rana, I.A., Khan, I.A., 2016. Assessment of Bt cotton genotypes for the Cry1Ac transgene and its expression. The Journal of Agricultural Science, 154(1): 109-117.
  8. Christou, P., Ford, T.L., 1995. The impact of selection parameters on the phenotype and genotype of transgenic rice callus and plants. Transgenic Research, 4(1): 44-51.
  9. Feng, C., Yuan, J., Wang, R., Liu, Y., Birchler, J.A., Han, F., 2016. Efficient targeted genome modification in maize using CRISPR/Cas9 system. Journal of Genetics and Genomics, 43(1): 37-43.
  10. Gryson, N., 2010. Effect of food processing on plant DNA degradation and PCR-based GMO analysis: a review. Analytical and Bioanalytical Chemistry, 396(6): 2003-2022.
  11. Holst-Jensen, A., Ronning, S.B., Lovseth, A., Berdal, K.G., 2003. PCR technology forscreening and quantifica