Genome-wide identification and molecular evolution of elongation family of very long chain fatty acids proteins in Cyrtotrachelus buqueti.

BMC Genomics

Key Laboratory of Sichuan Province for Bamboo Pests Control and Resource Development, Leshan Normal University, No. 778 Binhe Road, Shizhong District, Leshan, Sichuan, 614000, China.

Published: August 2024

AI Article Synopsis

  • Researchers identified 15 elongation family very long chain fatty acid (ELO) proteins in the genome of Cyrtotrachelus buqueti, distributed across four chromosomes, with an alkaline nature and primarily α-helix structures.
  • Developmental transcriptome analysis revealed key roles for specific CbuELO genes in synthesizing very long chain fatty acids in different life stages and under varying temperature conditions, while one gene consistently showed downregulation during feeding periods.
  • Protein-protein interaction analysis indicated that several CbuELO proteins are interrelated, providing insights into their molecular functions and interactions during the growth and development of C. buqueti.

Article Abstract

To reveal the molecular function of elongation family of very long chain fatty acids(ELO) protein in Cyrtotrachelus buqueti, we have identified 15 ELO proteins from C.buqueti genome. 15 CbuELO proteins were located on four chromosomes. Their isoelectric points ranged from 9.22 to 9.68, and they were alkaline. These CbuELO proteins were stable and hydrophobic. CbuELO proteins had transmembrane movement, and had multiple phosphorylation sites. The secondary structure of CbuELO proteins was mainly α-helix. A total of 10 conserved motifs were identified in CbuELO protein family. Phylogenetic analysis showed that molecular evolutionary relationships of ELO protein family between C. buqueti and Tribolium castaneum was the closest. Developmental transcriptome analysis indicated that CbuELO10, CbuELO13 and CbuELO02 genes were key enzyme genes that determine the synthesis of very long chain fatty acids in pupae and eggs, CbuELO6 and CbuELO7 were that in the male, and CbuELO8 and CbuELO11 were that in the larva. Transcriptome analysis under different temperature conditions indicated that CbuELO1, CbuELO5, CbuELO12 and CbuELO14 participated in regulating temperature stress responses. Transcriptome analysis at different feeding times showed CbuELO12 gene expression level in all feeding time periods was significant downregulation. The qRT-PCR experiment verified expression level changes of CbuELO gene family under different temperature and feeding time conditions. Protein-protein interaction analysis showed that 9 CbuELO proteins were related to each other, CbuELO1, CbuELO4 and CbuELO12 had more than one interaction relationship. These results lay a theoretical foundation for further studying its molecular function during growth and development of C. buqueti.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11297609PMC
http://dx.doi.org/10.1186/s12864-024-10658-8DOI Listing

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