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Sago Palm Genome Size Estimation via Real-Time Quantitative PCR

Sago Palm Genome Size Estimation Via Real-Time Quantitative PCR

Original Research ArticleFeb 27, 2020Vol. 20 No. 2 (2020)

Abstract

Sago palm, Metroxylon sagu Rottb., is an underutilized indigenous food crop that can be found mainly in the South East Asia and Pacific regions. It is a main starch producer and socioeconomically important crop in the South East Asia region including Malaysia. The sago starch provides foronsiderable potential to food security in the places where it is grown. However, not many molecular works have been reported thus far. In the post genomic era, sago plant genome sequencing is very important for sustainable starch development in these regions. Therefore, determination of the genome size is prerequisite to full genome sequencing and assembly. Here we report on the use of real-time quantitative polymerase chain reaction (qPCR) in determining the genome size. For this work, we calculated the genome size, G (bp) of M. sagu based on qPCR-derived copy number of two single copy genes. Pichia pastorisas a control to estimate sago palm genome size. With this technique, the genome size of M. sagu was calculated to be 1.87 Gbp. This genome size information would be beneficial for subsequent molecular work including genome sequencing and analysis on this economically important crop plant.

 

Keywords: Genome size; Metroxylon sagu; real-time PCR; copy number; Pichia pastoris

*Corresponding author: Tel.: +60 82 58 3038   Fax: +60 82 58 3160

             E-mail: hairulroslan@hotmail.com

How to Cite

Roslan*, H. undefined. A. ., Hossain, M. undefined. A. ., Sing, N. undefined. N. ., & Husaini, A. undefined. . (2020). Sago Palm Genome Size Estimation via Real-Time Quantitative PCR. CURRENT APPLIED SCIENCE AND TECHNOLOGY, 208-216.

References

  • Wee, C.C. and Roslan, H.A., 2012. Expressed sequence tags (ESTs) from young leaves of Metroxylon sagu. 3 Biotech, 2, 211-218.
  • Hare, E.E. and Johnston, J.S., 2011. Genome size determination using flow cytometry of propidium iodide-stained nuclei. Methods in Molecular Biology, 772, 3-12.
  • Zhang, J.Z. and Fan M.Y., 2002. Determination of genome size and restriction fragment length polymorphism of four Chinese rickettsial isolates by pulsed-field gel electrophoresis. Acta Virologica, 46, 25-30.
  • D’Hondt, L., Hofte, M., Van Bockstaele, E. and Leus, L., 2011. Applications of flow cytometry in plant pathology for genome size determination, detection and physiological status. Molecular Plant Pathology, 12, 815-828.
  • Mounsey, K.E., Willis, C., Burgess, S.T.G., Holt, D.C., McCarthy, J. and Fischer, K., 2012. Quantitative PCR-based genome size estimation of the astigmatid mites Sarcoptes scabiei, Psoroptes ovis and Dermatophagoides pteronyssinus. Parasites & Vectors, 5, 3. https://doi.org/10.1186/1756-3305-5-3.

Author Information

Hairul Azman Roslan*

Faculty of Resource Science and Technology, Universiti Malaysia Sarawak, Sarawak, Malaysia

Md Anowar Hossain

Department of Biochemistry and Molecular Biology, University of Rajshahi, Bangladesh

Ngieng Ngui Sing

Faculty of Resource Science and Technology, Universiti Malaysia Sarawak, Sarawak, Malaysia

Ahmad Husaini

Faculty of Resource Science and Technology, Universiti Malaysia Sarawak, Sarawak, Malaysia

About this Article

Journal

Vol. 20 No. 2 (2020)

Type of Manuscript

Original Research Article

Keywords

Genome size; Metroxylon sagu; real-time PCR; copy number; Pichia pastoris

Published

27 February 2020