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. 2022 Jun;28(6):1147-1158.
doi: 10.1007/s12298-022-01204-5. Epub 2022 Jul 6.

Identification and expression analysis of chlorophyll a/b binding protein gene family in grape (Vitis vinifera)

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Identification and expression analysis of chlorophyll a/b binding protein gene family in grape (Vitis vinifera)

Yunchun Wei et al. Physiol Mol Biol Plants. 2022 Jun.

Abstract

In higher plants, light capture of chlorophyll a/b binding protein (Lhc) plays a crucial role in the plant's response to adverse environment. So far, the family has not been systematically identified in grapes. In this study, 20 VvLhcs were identified in the grape genome, which were distributed in 13 of 19 grape chromosomes and divided into 7 developing branches. The results of gene duplication analysis showed that 6 VvLhcs formed fragment duplication events, while there was no tandem duplication in VvLhcs. Exon-intron structure analysis showed that they had a wide number of exons. Protein conserved motif analysis showed that VvLhcs contained more similar motif structures in the same phylogenetic branch. The cis-acting elements in the VvLhcs promoter region mainly respond to light, plant hormones and abiotic stresses. In addition, qRT-PCR results showed that different proportions of salt stress and red-blue light affected the expression of VvLhcs and the expression patterns of genes in different grape varieties were different. The results for further study on different grape varieties in different combinations of red and blue light of the Lhc provide a theoretical basis.

Supplementary information: The online version contains supplementary material available at 10.1007/s12298-022-01204-5.

Keywords: Gene family identification; Grape; Lhc; Red-blue light; Salt stress.

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Conflict of interest statement

Conflict of interestThe authors declare no conflict of interest.

Figures

Fig. 1
Fig. 1
Phylogenetic relationship of grape Lhcs and other plants. The phylogenetic tree was constructed using 20 grape, 21 Arabidopsis, and 20 cassava Lhc proteins sequences
Fig. 2
Fig. 2
Schematic representation of VvLhcs. A Based on the total amino acids of 20 VvLhc proteins, the phylogenetic tree was constructed by the adjacency method realized by MEGA software. B Gene structures of the 20 VvLhcs. The exons and introns were marked by yellow rectangles and thin lines, respectively. The untranslated regions (UTRs) were indicated by blue rectangles. C Motifs of the VvLhc proteins were identified using the online MEME program. Different colors boxes represented different motifs
Fig. 3
Fig. 3
The distribution of VvLhc on grape chromosomes
Fig. 4
Fig. 4
The number of stress-responsive cis-acting elements in the promoter region of each VvLhc
Fig. 5
Fig. 5
The expression profiles of VvLhc in 6 different grape organs and tissues. Expression data corresponding to 20 grape VvLhc was retrieved from the international bio-analytic resource for plant biology (BAR) data sets for further analysis. The heat map was generated based on the RPKM (Reads Per Kilobase of exon model per million mapped reads) values that were transformed to log2 (value + 1). Red and blue color gradients indicate an increase or decrease, respectively
Fig. 6
Fig. 6
The expression levels of 20 VvLhcs in grape leaves under NaCl treatment. Each value is expressed as the mean ± SD (n = 3, 3 biological replicates × 3 technical replicates). Different lowercase letters represent significant differences (P ≤ 0.05)

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References

    1. Alboresi A, Caffarri S, Nogue F, Bassi R, Morosinotto T. In silico and biochemical analysis of Physcomitrella patens photosynthetic antenna: identification of subunits which evolved upon land adaptation. PLoS ONE. 2008;3:e2033. doi: 10.1371/journal.pone.0002033. - DOI - PMC - PubMed
    1. Broglie R, Bellemare G, Bartlett SG, Chua NH, Cashmore AR. Cloned DNA sequences complementary to mRNAs encoding precursors to the small subunit of ribulose-1,5-bisphosphate carboxylase and a chlorophyll a/b binding polypeptide. Proc Natl Acad Sci USA. 1981;78:7304–7308. doi: 10.1073/pnas.78.12.7304. - DOI - PMC - PubMed
    1. Brunner H, Rüdiger W. The greening process in cress seedlings IV. Light regulated expression of single Lhc genes. J Photochem Photobiol B Biol. 1995;27:257–263. doi: 10.1016/1011-1344(94)07076-Z. - DOI
    1. Cannon SB, Mitra A, Baumgarten A, Young ND, May G. The roles of segmental and tandem gene duplication in the evolution of large gene families in Arabidopsis thaliana. BMC Plant Biol. 2004;4:10. doi: 10.1186/1471-2229-4-10. - DOI - PMC - PubMed
    1. Chattopadhyay S, Ang LH, Puente P, Deng XW, Wei N. Arabidopsis bZIP protein HY5 directly interacts with light-responsive promoters in mediating light control of gene expression. Plant Cell. 1998;10:673–683. doi: 10.1105/tpc.10.5.673. - DOI - PMC - PubMed

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