Acta Biologica
Previously: Zeszyty Naukowe Uniwersytetu Szczecińskiego. Acta Biologica
Bioinformatics analysis of the promoter sequence of the 9f-2.8 gene encoding germin
DOI: 10.18276/ab.2018.25-11
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| ISSN: | 2450-8330 |
| eISSN: | 2353-3013 |
| Authors: |
Izabela
Szućko
University of Szczecin, Institute for Research on Biodiversity, Faculty of Biology, Department of Molecular Biology and Cytology Urszula Kowalska University of Szczecin, Institute for Research on Biodiversity, Faculty of Biology, Department of Molecular Biology and Cytology Lidia Skuza University of Szczecin, Institute for Research on Biodiversity, Faculty of Biology, Department of Molecular Biology and Cytology |
| Keywords: | Triticum aestivum L. bioinformatic tools germin protein in silico analyse |
| Issue / book publication date: | 2018 |
| Page range: | 9 (131-139) |
| OAI-PMH: | Metadata |
| Cited-by (Crossref) ?: | Enable JavaScript to retrieve citation data. |
Abstract
Bioinformatics is a field of study having an enormous potential, allowing to solve a number
of problems arising as a result of dynamic development of natural sciences with the use
of computer science methodologies. It is widely used and constitutes a basis for most scientific
research conducted in the field of molecular biology. The aim of this study was in silico analysis
of the promoter sequence of the 9f-2.8 gene encoding isoform of the germin protein considered
as a germination marker in common wheat’s (Triticum aestivum L.). The gene mentioned
above has already been characterized, however, with the use of experimental methods instead
of bioinformatics. Analysis with the use of TSSP and TSSPlant software identified the promoter
region and classified it as the TATA-box containing promoter. For 9f-2.8 gene including 2.8
kbp, the TSSP software indicated that the TATA-box sequence was located in the position 1665
nt, while the TSSPlant tool showed that TSS [+1] was located in the position 1699 nt. At the
second stage, transcription factors were analyzed. Four main families of transcription factors
were detected within the analyzed region: MADS, AP2, bZIP and NAC. The most common
were MADS-box and bZIP motifs. In the final step of analysis the presence of CpG islands have
been checked using the PlantPAN software. The region which could be potentially considered
as CpG island have been detected and localized. Software used in analysis above is free online
tool.
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