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Differential Gene Expression and Metabolic Pathway Analysis of Cladophora rupestris under Pb Stress Conditions

This study aimed to analyze the transcriptome of C. rupestris under Pb(2+) stress by using high-throughput sequencing technology, observe the changes of gene expression and metabolic pathway after three and five days under 1.0 and 5.0 mg/L of Pb(2+) treatment, and analyze the differentially expresse...

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Detalles Bibliográficos
Autores principales: Liu, Lei, Zhang, Lusheng, Zhao, Lingyun, Chen, Qiuyu, Zhang, Qian, Cao, Deju, Liu, Zhaowen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656615/
https://www.ncbi.nlm.nih.gov/pubmed/36360789
http://dx.doi.org/10.3390/ijerph192113910
Descripción
Sumario:This study aimed to analyze the transcriptome of C. rupestris under Pb(2+) stress by using high-throughput sequencing technology, observe the changes of gene expression and metabolic pathway after three and five days under 1.0 and 5.0 mg/L of Pb(2+) treatment, and analyze the differentially expressed genes (DEGs) and related functional genes after Pb(2+) treatment. Metabolic pathways were revealed through Gene Ontology (GO) and the Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis. Results show that DEGs increased significantly with the increase of Pb(2+) concentration and stress time. A total of 32 genes were closely related to Pb(2+) stress response. GO analysis identified two major transporter proteins, namely, ATP-binding transport protein-related (ABC transporters) and zinc finger CCHC domain containing protein (Zfp) in C. rupestris. Pthr19248, pthr19211, Zfp pthr23002, Zfp p48znf pthr12681, Zfp 294 pthr12389, and Zfp pthr23067 played important roles against Pb(2+) toxicity and its absorption in C. rupestris. KEGG pathway analysis suggested that ABCA1, ATM, and ABCD3 were closely related to Pb(2+) absorption. Pb(2+) stress was mainly involved in metallothionein (MT), plant hormone signal transduction, ABC transporters, and glutathione (GSH) metabolism.