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    Genetic structure analysis of 121 wild goji berry germplasms based on SSR fluorescence markers
    DAI Guo-li, LIU Na, QIN Ken, ZHANG Bo, YIN Yue, MI Ja, HE Xin-ru
    HUBEI AGRICULTURAL SCIENCES    2024, 63 (5): 207-214.   DOI: 10.14088/j.cnki.issn0439-8114.2024.05.036
    Abstract230)      PDF (4891KB)(63)       Save
    121 wild goji berry(Lycium barbarum L.) germplasms were collected as materials, 9 pairs of SSR primers were used of amplification, and polymorphism was analyzed using GeneALEX and Power Marker software. Genetic diversity analysis, cluster analysis, and principal component analysis were performed using NTSYS and STRUC-TURE software.The results showed that a total of 108 alleles were detected using 9 pairs of SSR primers. The number of alleles (Na), effective alleles (Ne), observed heterozygosity (Ho), expected heterozygosity (He), polymorphic information content (PIC), and Shannon’s information index were 12, 4.620, 0.678, 0.651, 0.629, and 1.568, respectively;the clustering results showed that 121 wild goji berry germplasms could be divided into 5 subgroups. The genetic structure of the population showed that when K=5, 121 germplasms could be divided into 5 subgroups. The genetic distance between NXGY-02 and NXGY-03 germplasms from Ningxia and 6 germplasms from Inner Mongolia was the farthest, and the genetic relationship was relatively distant,there was extensive gene exchange among other wild goji berry germplasms from Qinghai Province, Xinjiang, Gansu Province, and Inner Mongolia;the wild goji berry germplasms in Ningxia and Inner Mongolia had the possibility of independent origin and evolution, while the germplasms in Xinjiang, Gansu, and Qinghai provinces were closely related to the germplasms in Ningxia and were likely to belong to the same origin.
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    Identification of the MYB family of Actinidia deliciosa and its response to flooding stress
    YUE You-zhang, WANG Jian-jun, JI Xiao-mei, CHI Wen-chao, LIN Zhi-xi
    HUBEI AGRICULTURAL SCIENCES    2024, 63 (5): 215-222.   DOI: 10.14088/j.cnki.issn0439-8114.2024.05.037
    Abstract211)      PDF (7700KB)(28)       Save
    Based on the second-generation transcriptome sequencing data of Actinidia deliciosa, AcMYB family genes were identified and analyzed using various bioinformatics methods. The results showed that a total of 64 AcMYB family members with complete ORF sequences were obtained from the transcriptome data of Actinidia deliciosa, which were divided into 4 subgroups. Among them, subgroup I had 34 members, subgroup II had 18 members, subgroup III had 10 members, and subgroup IV had 2 members. Expression analysis before and after waterlogging treatment showed that the expression levels of AcMYB members such as AcMYB214187 and AcMYB25788 were significantly reduced in the roots of Actinidia deliciosa, responding quickly to waterlogging stress, while there was no significant difference in expression levels in the leaves. The expression levels in the roots of AcMYB members such as AcMYB19450 and AcMYB30021 were not significantly different, but the expression levels in the leaves were significantly reduced. This might be due to the fact that the roots, upon receiving hypoxic stress signals, transmitted them to the aboveground parts and exerted their effects, regulating the response of Actinidia deliciosa to hypoxic stress at the transcriptional level. The research results provided a basis for further research on MYB transcription factors in Actinidia deliciosa, promoting stress resistance breeding, and improving yield.
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