Journals / Turkish Journal of Biology / 2019 / Cilt: 43 - Sayı: 6

Identification of watermelon heat shock protein members and tissue-specific gene expression analysis under combined drought and heat stresses

Pages
404–419
Publication Date
2022-10-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

This study provides extensive information for watermelon Hsps, and can enhance our knowledge about therelationships between Hsp genes and combined stresses.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Heat shock protein (Hsp) gene family members in the watermelon genome were identified and characterized by bioinformaticsanalysis.
📊
Key Findings & Data:In addition, expression profiles of genes under combined drought and heat stress conditions were experimentally analyzed.In the watermelon genome, 39 genes belonging to the sHsp family, 101 genes belonging to the Hsp40 family, 23 genes belonging to theHsp60 family, 12 genes belonging to the Hsp70 family, 6 genes belonging to the Hsp90 family, and 102 genes belonging to the Hsp100family were found.
💡
Conclusion & Impact:This study provides extensive information for watermelon Hsps, and can enhance our knowledge about therelationships between Hsp genes and combined stresses.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Heat shock protein (Hsp) gene family members in the watermelon genome were identified and characterized by bioinformaticsanalysis. In addition, expression profiles of genes under combined drought and heat stress conditions were experimentally analyzed.In the watermelon genome, 39 genes belonging to the sHsp family, 101 genes belonging to the Hsp40 family, 23 genes belonging to theHsp60 family, 12 genes belonging to the Hsp70 family, 6 genes belonging to the Hsp90 family, and 102 genes belonging to the Hsp100family were found. It was also observed that the proteins in the same cluster in the phylogenetic trees had similar motif patterns. Whenthe estimated 3-dimensional structures of the Hsp proteins were examined, it was determined that the α-helical structure was dominantin almost all families. The most orthologous relationship appeared to be between watermelon, soybean, and poplar in the ClaHsp genefamilies. For tissue-specific gene expression analysis under combined stress conditions, expression analysis of one representative Hspgene each from root, stem, leaf, and shoot tissues was performed by real-time PCR. A significant increase was detected usually at 30min in almost all tissues. This study provides extensive information for watermelon Hsps, and can enhance our knowledge about therelationships between Hsp genes and combined stresses.

🔖

Cite This Article

KELEŞ, M., CAN, T. H., BALOĞLU, M. C., ALTUNOĞLU, Y. Ç. (2022). Identification of watermelon heat shock protein members and tissue-specific gene expression analysis under combined drought and heat stresses. Turkish Journal of Biology, Cilt: 43 - Sayı: 6, 404–419. https://ajindex.com/articles/600229

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (10)

  1. Al-Whaibi MH (2011). Plant heat-shock proteins: A mini review. Journel of King Saud University-Science 23: 139-150.
  2. Bailey TL, Johnson J, Grant CE, Noble WS (2015). The MEME Suite. Nucleic Acids Research 43: W39-49. Baloğlu MC, Eldem V, Hajyzadeh M, Unver T (2014a). Genome-wide analysis of the bZIP transcription factors in cucumber. PLoS ONE 9 (4): e96014. Baloğlu MC (2014b). Genome-wide in silico identification and comparison of Growth Regulating Factor (GRF) genes in the Cucurbitaceae family. Plant Omics Journal 7 (4): 260-270.
  3. Baloğlu MC, Patir MG (2014c). Molecular characterization, 3D model analysis, and expression pattern of the CmUBC gene encoding the melon ubiquitin-conjugating enzyme under drought and salt stress conditions. Biochemical Genetics 52: 90-105.
  4. Baloğlu MC, Inal B, Kavas M, Unver T (2014d). Diverse expression pattern of wheat transcription factors against abiotic stresses in wheat species. Gene 550 (1): 117-122.
  5. Baloğlu MC, Ulu F, Altunoğlu YC, Pekol S, Alagoz G et al. (2015). Identification, molecular characterization and expression analysis of RPL24 genes in three Cucurbitaceae family members: cucumber, melon and watermelon. Biotechnology & Biotechnological Equipment 29: 1024-1034.
  6. Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN et al. (2000). The Protein Data Bank. Nucleic Acids Research 28 (1): 235-242.
  7. Budak H Akpinar AB (2015). Plant miRNAs: biogenesis, organization and origins. Functional and Integrative Genomics 15 (5): 523- 531. Büyük I, Fazlioğlu A, Aras S (2012). Relation between different concentrations of Cd+2 treatment and mRNA levels of 17.7 kDa heat-shock protein gene in Helianthus annuus plants. Journal of Biotechnology 161: 45. Büyük İ, Soydam-Aydın S, Aras S (2012). Bitkilerin stres koşullarına verdiği moleküler cevaplar. Türk Hijyen ve Deneysel Biyoloji 69 (2): 97-110.
  8. Cao F, Cheng H, Cheng S, Li L, Xu F et al. (2012). Expression of selected ginkgo biloba heat shock protein genes after cold treatment could be induced by other abiotic stress. International Journal of Molecular Sciences 13 (5): 5768-5788.
  9. Collins JK, Wu G, Perkins-Veazie P, Spears K, Claypool PL et al. (2007). Watermelon consumption increases plasma arginine concentrations in adults. Nutrition 23 (3): 261-266.
  10. Conesa A, Götz S (2008). Blast2GO: A comprehensive suite for functional analysis in plant genomics. International Journal of Plant Genomics 2008: 12. Çelik Altunoğlu Y (2016a). Isı Şoku Protein Ailesinden Hsp70 Genlerinin Okaliptüs Genomund