Evidence map›Paper›PMID 39179324›Full record

ArticleJournal, genetic engineering & biotechnology2024

Analysis of promoter region and regulatory elements of Rhizobium giardinii DNA-binding response regulator A3AY_RS01 genes.

Genet Atsbeha, Mulugeta Kebede, Behailu Samuel, Haftom Baraki, Hailekiros Tadesse, Desta Berhe Sbhatu

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Article in Journal, genetic engineering & biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Genet AtsbehaDepartment of Applied Biology, School of Applied Natural Science, Adama Science and Technology University, Adama, Ethiopia. Electronic address: genet.atsbeha@astu.edu.et.
Mulugeta KebedeDepartment of Plant Biology and Biodiversity Management, Addis Ababa University, Addis Ababa, Ethiopia. Electronic address: mulugeta.kebede@astu.edu.et.
Behailu SamuelDepartment of Animal Science, College of Agriculture and Natural Resource, Salale University, Fitche, Ethiopia. Electronic address: behailus2001@gmail.com.
Haftom BarakiDepartment of Biological and Chemical Engineering, Mekelle Institute of Technology, Mekelle University, Mekelle, Ethiopia. Electronic address: hbarakibiot@gmail.com.
Hailekiros TadesseDepartment of Biological and Chemical Engineering, Mekelle Institute of Technology, Mekelle University, Mekelle, Ethiopia. Electronic address: hailekiros.tadesse@mu.edu.et.
Desta Berhe SbhatuDepartment of Biological and Chemical Engineering, Mekelle Institute of Technology, Mekelle University, Mekelle, Ethiopia. Electronic address: desta.sbhatu@mu.edu.et.

Funding

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6 · The paper itself

Abstract

backgroundRhizobium giardinii has been demonstrated to colonize the roots of a variety of legume species, including common beans, and to increase nitrogen fixation. This suggests that Rhizobium giardinii might be a beneficial tool for sustainable agriculture by lowering dependency on synthetic nitrogen fertilizers and enhancing soil fertility. Understanding the regulatory components in the R. giardinii A3AY_RS01 genes might also lead to the creation of innovative ways for increasing the effectiveness of nitrogen fixation in other agriculturally important bacteria. Therefore, this study was aimed to predict regulatory element of R. giardinii DNA-binding response regulator A3AY_RS01 genes.

resultsThe locations for 19 % of the Transcriptional start site (TSSs) were within -300 bp relative to the start codon and ten candidate motifs were identified that are shared by at least 50 % of the R. giardinii A3AY_RS01 promoter input sequences from both strands. Motif 1 was revealed as the common promoter motif for all of R. giardinii A3AY_RS01 genes that serves as binding sites for TFs involved in the expression regulation of these genes. Hence, it was revealed that Motif 1 may serve as the binding site chiefly for Ferric uptake regulator (Fur) transcription factor family to regulate expression of A3AY_RS01 genes. High CpG density in the promoter than body regions were observed for most of the genes except for A3AY_RS0102950, A3AY_RS0120195 and A3AY_RS0131150 genes. Nonetheless, promoter areas were richer than body regions in both techniques.

conclusionsMV1 motif can serve as a binding site for the Fur transcription factor gene family in R. giardinii to regulate the expression of R. giardinii A3AY_RS01 genes. R. giardinii A3AY_RS01 genes are rich in CpG Islands, and play an important role in the regulation of the gene expression of nitrogen fixing in this bacterium.

Indexed as

FerricNitrogen fixing bacteriaTranscriptional FactorsTranscriptional Start SiteUptake regulator

Identifiers

PMID39179324
PMCPMC11231716

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