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Cloning and Expression Analysis of SnRK1 in Actinidia chinensis var. Hongyang
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Kaixiu JIANG1, 2, Linya LIU2, Bin HE2, Shuyi SONG2, Xiaojian GONG1, *, Yacheng HUANG2, *
Chinese Journal of Tropical Crops | 2025, 46(2) : 300 - 309
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Chinese Journal of Tropical Crops | 2025, 46(2): 300-309
Omics & Biotechnology
Cloning and Expression Analysis of SnRK1 in Actinidia chinensis var. Hongyang
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Kaixiu JIANG1, 2, Linya LIU2, Bin HE2, Shuyi SONG2, Xiaojian GONG1, *, Yacheng HUANG2, *
Affiliations
  • 1.Key Laboratory for Information System of Mountainous Areas and Protection of Ecological Environment, Guizhou Normal University, Guiyang, Guizhou 550001, China
  • 2.School of Biological Science and Technology, Liupanshui Normal University, Liupanshui, Guizhou 553004, China
Published: 2025-02-25 doi: 10.3969/j.issn.1000-2561.2025.02.006
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Hongyang kiwifruit is a distinguished variety independently developed in China. It features a distinctive red coloration, possesses high sugar content and low acidity, and is favored for its rich aroma and unique flavor profile. The growth and development of fruits are influenced by a multitude of factors, among which sucrose non-fermentation-1-associated protein kinase 1 (SnRK1) plays a pivotal role in the regulation of carbohydrate metabolism and the response to both biotic and abiotic stresses. Therefore, in this study, we cloned the full-length cDNA of 2 genes in the SnRK1 family of Hongyang kiwifruit, named AcSnRK1.1 and AcSnRK1.2. The physical and chemical properties, gene structure, conserved motifs, protein conserved domains, and cis-acting elements of AcSnRK1.1 and AcSnRK1.2 were systematically analyzed using bioinformatics approaches. The expression characteristics of AcSnRK1.1 and AcSnRK1.2 genes in different tissues and fruits were quantitatively detected by real-time fluorescence. AcSnRK1.1 and AcSnRK1.2 genes contained an open reading frame of 1548 bp and 1545 bp, respectively, encoding proteins containing 515 and 514 amino acids with highly consistent sequences (96.31%) respectively. Both genes contained 10 exons and 2 introns. Bioinformatics analysis showed that AcSnRK1.1 and AcSnRK1.2 had high homology with other plant SnRK1 proteins. The amino acid sequence showed that STKc_AMPK_alpha, AMPK_C and UBA_SnRK1_plant were unique to the SnRK1 family. Evolutionary tree analysis showed that AcSnRK1.1 and AcSnRK1.2 belonged to the SnRK1 family. Tissue specific analysis showed that AcSnRK1.1 and AcSnRK1.2 were expressed in all tissues of Hongyang Kiwifruit, but the expression abundance was the highest in fruit. During fruit development, the expression levels of AcSnRK1.1 and AcSnRK1.2 decreased first and then increased. qRT-PCR analysis showed that the expression of AcSnRK1.1 and AcSnRK1.2 was responsive to ABA, GA3, ET and CPPU. With the increase of storage time, the expression levels of AcSnRK1.1 and AcSnRK1.2 showed a downward trend first and then an upward trend, suggesting that AcSnRK1 gene might regulate the expression of sucrose synthase. The results of this study indicate that AcSnRK1.1 and AcSnRK1.2 genes play an important role in the development and storage of Hongyang kiwifruit, which would lay a foundation for further elucidation of the functions of AcSnRK1.1 and AcSnRK1.2 genes.

Actinidia chinensis var. Hongyang  /  SnRK1  /  gene cloning  /  bioinformatics analysis  /  expression analysis
Kaixiu JIANG, Linya LIU, Bin HE, Shuyi SONG, Xiaojian GONG, Yacheng HUANG. Cloning and Expression Analysis of SnRK1 in Actinidia chinensis var. Hongyang[J]. Chinese Journal of Tropical Crops, 2025 , 46 (2) : 300 -309 . DOI: 10.3969/j.issn.1000-2561.2025.02.006
Year 2025 volume 46 Issue 2
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doi: 10.3969/j.issn.1000-2561.2025.02.006
  • Receive Date:2024-09-04
  • Online Date:2026-06-23
  • Published:2025-02-25
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  • Received:2024-09-04
  • Revised:2024-09-24
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Affiliations
    1.Key Laboratory for Information System of Mountainous Areas and Protection of Ecological Environment, Guizhou Normal University, Guiyang, Guizhou 550001, China
    2.School of Biological Science and Technology, Liupanshui Normal University, Liupanshui, Guizhou 553004, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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