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Cloning and Functional Characterization of SpZIP2.
Han, Tian-Long; Tang, Ting-Wei; Zhang, Pei-Hong; Liu, Min; Zhao, Jing; Peng, Jia-Shi; Meng, Shuan.
Affiliation
  • Han TL; College of Agronomy, Hunan Agricultural University, Changsha 410128, China.
  • Tang TW; College of Agronomy, Hunan Agricultural University, Changsha 410128, China.
  • Zhang PH; School of Life and Health Sciences, Hunan University of Science and Technology, Xiangtan 411201, China.
  • Liu M; Xiaoxiang College, Hunan University of Science and Technology, Xiangtan 411201, China.
  • Zhao J; College of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China.
  • Peng JS; School of Life and Health Sciences, Hunan University of Science and Technology, Xiangtan 411201, China.
  • Meng S; College of Agronomy, Hunan Agricultural University, Changsha 410128, China.
Genes (Basel) ; 13(12)2022 12 17.
Article in En | MEDLINE | ID: mdl-36553665
ABSTRACT
Zinc (Zn)-regulated and iron (Fe)-regulated transporter-like proteins (ZIP) are key players involved in the accumulation of cadmium (Cd) and Zn in plants. Sedum plumbizincicola X.H. Guo et S.B. Zhou ex L.H. Wu (S. plumbizincicola) is a Crassulaceae Cd/Zn hyperaccumulator found in China, but the role of ZIPs in S. plumbizincicola remains largely unexplored. Here, we identified 12 members of ZIP family genes by transcriptome analysis in S. plumbizincicola and cloned the SpZIP2 gene with functional analysis. The expression of SpZIP2 in roots was higher than that in the shoots, and Cd stress significantly decreased its expression in the roots but increased its expression in leaves. Protein sequence characteristics and structural analysis showed that the content of alanine and leucine residues in the SpZIP2 sequence was higher than other residues, and several serine, threonine and tyrosine sites can be phosphorylated. Transmembrane domain analysis showed that SpZIP2 has the classic eight transmembrane regions. The evolutionary analysis found that SpZIP2 is closely related to OsZIP2, followed by AtZIP11, OsZIP1 and AtZIP2. Sequence alignment showed that most of the conserved sequences among these members were located in the transmembrane regions. A further metal sensitivity assay using yeast mutant Δyap1 showed that the expression of SpZIP2 increased the sensitivity of the transformants to Cd but failed to change the resistance to Zn. The subsequent ion content determination showed that the expression of SpZIP2 increased the accumulation of Cd in yeast. Subcellular localization showed that SpZIP2 was localized to membrane systems, including the plasma membrane and endoplasmic reticulum. The above results indicate that ZIP member SpZIP2 participates in the uptake and accumulation of Cd into cells and might contribute to Cd hyperaccumulation in S. plumbizincicola.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saccharomyces cerevisiae / Cadmium Type of study: Prognostic_studies Language: En Journal: Genes (Basel) Year: 2022 Document type: Article Affiliation country: China Publication country: CH / SUIZA / SUÍÇA / SWITZERLAND

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Saccharomyces cerevisiae / Cadmium Type of study: Prognostic_studies Language: En Journal: Genes (Basel) Year: 2022 Document type: Article Affiliation country: China Publication country: CH / SUIZA / SUÍÇA / SWITZERLAND