Functional verification of the JmLFY gene associated with the flowering of Juglans mandshurica Maxim
In this study, a pBI121- plant expression vector was constructed on the basis of obtaining the full-length sequence of the gene from , which was then used for genetic transformation inflorescence infection using wild-type and mutants as transgenic receptors. Seeds of positive plants with high expres...
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Published in | PeerJ (San Francisco, CA) Vol. 11; p. e14938 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Abstract | In this study, a pBI121-
plant expression vector was constructed on the basis of obtaining the full-length sequence of the
gene from
, which was then used for genetic transformation
inflorescence infection using wild-type
and
mutants as transgenic receptors. Seeds of positive
plants with high expression of
were collected and sowed till the homozygous T3 regeneration plants were obtained. Then the expression of flowering-related genes (
,
,
and
) in T3 generation plants were analyzed and the results showed that
gene overexpression promoted the expression of flowering-related genes and resulted in earlier flowering in
. The
plants of
-transformed and
-transformed
mutants appeared shorter leaves, longer fruit pods, and fewer cauline leaves than those of wild-type and the
mutants plants, respectively. In addition, some secondary branches in the transgenic plants converted into inflorescences, which indicated that the overexpression of
promoted the transition from vegetative growth to reproductive growth, and compensate the phenotypic defects of
mutant partially. The results provides a scientific reference for formulating reasonable genetic improvement strategies such as shortening childhood, improving yield and quality, and breeding desirable varieties, which have important guiding significance in production. |
---|---|
AbstractList | In this study, a pBI121-JmLFY plant expression vector was constructed on the basis of obtaining the full-length sequence of the JmLFY gene from Juglans mandshurica, which was then used for genetic transformation via Agrobacterium inflorescence infection using wild-type Arabidopsis thaliana and lfy mutants as transgenic receptors. Seeds of positive A. thaliana plants with high expression of JmLFY were collected and sowed till the homozygous T3 regeneration plants were obtained. Then the expression of flowering-related genes (AtAP1, AtSOC1, AtFT and AtPI) in T3 generation plants were analyzed and the results showed that JmLFY gene overexpression promoted the expression of flowering-related genes and resulted in earlier flowering in A. thaliana. The A. thaliana plants of JmLFY-transformed and JmLFY-transformed lfy mutants appeared shorter leaves, longer fruit pods, and fewer cauline leaves than those of wild-type and the lfy mutants plants, respectively. In addition, some secondary branches in the transgenic plants converted into inflorescences, which indicated that the overexpression of JmLFY promoted the transition from vegetative growth to reproductive growth, and compensate the phenotypic defects of lfy mutant partially. The results provides a scientific reference for formulating reasonable genetic improvement strategies such as shortening childhood, improving yield and quality, and breeding desirable varieties, which have important guiding significance in production. In this study, a pBI121- JmLFY plant expression vector was constructed on the basis of obtaining the full-length sequence of the JmLFY gene from Juglans mandshurica , which was then used for genetic transformation via Agrobacterium inflorescence infection using wild-type Arabidopsis thaliana and lfy mutants as transgenic receptors. Seeds of positive A. thaliana plants with high expression of JmLFY were collected and sowed till the homozygous T3 regeneration plants were obtained. Then the expression of flowering-related genes ( AtAP1 , AtSOC1 , AtFT and AtPI ) in T3 generation plants were analyzed and the results showed that JmLFY gene overexpression promoted the expression of flowering-related genes and resulted in earlier flowering in A. thaliana . The A. thaliana plants of JmLFY -transformed and JmLFY -transformed lfy mutants appeared shorter leaves, longer fruit pods, and fewer cauline leaves than those of wild-type and the lfy mutants plants, respectively. In addition, some secondary branches in the transgenic plants converted into inflorescences, which indicated that the overexpression of JmLFY promoted the transition from vegetative growth to reproductive growth, and compensate the phenotypic defects of lfy mutant partially. The results provides a scientific reference for formulating reasonable genetic improvement strategies such as shortening childhood, improving yield and quality, and breeding desirable varieties, which have important guiding significance in production. In this study, a pBI121- plant expression vector was constructed on the basis of obtaining the full-length sequence of the gene from , which was then used for genetic transformation inflorescence infection using wild-type and mutants as transgenic receptors. Seeds of positive plants with high expression of were collected and sowed till the homozygous T3 regeneration plants were obtained. Then the expression of flowering-related genes ( , , and ) in T3 generation plants were analyzed and the results showed that gene overexpression promoted the expression of flowering-related genes and resulted in earlier flowering in . The plants of -transformed and -transformed mutants appeared shorter leaves, longer fruit pods, and fewer cauline leaves than those of wild-type and the mutants plants, respectively. In addition, some secondary branches in the transgenic plants converted into inflorescences, which indicated that the overexpression of promoted the transition from vegetative growth to reproductive growth, and compensate the phenotypic defects of mutant partially. The results provides a scientific reference for formulating reasonable genetic improvement strategies such as shortening childhood, improving yield and quality, and breeding desirable varieties, which have important guiding significance in production. |
ArticleNumber | e14938 |
Audience | Academic |
Author | Dong, Tianyi Jia, Ruoxue Jiang, Ying Zhang, Lijie Cai, Jiayou Fu, Jingqi Deng, Jifeng |
Author_xml | – sequence: 1 givenname: Jiayou surname: Cai fullname: Cai, Jiayou organization: Key Laboratory of Forest Tree Genetics, Breeding and Cultivation of Liaoning Province, Shenyang, Liaoning, China – sequence: 2 givenname: Ruoxue surname: Jia fullname: Jia, Ruoxue organization: Shenyang Agricultural University, Shenyang, Liaoning, China – sequence: 3 givenname: Ying surname: Jiang fullname: Jiang, Ying organization: Shenyang Agricultural University, Shenyang, Liaoning, China – sequence: 4 givenname: Jingqi surname: Fu fullname: Fu, Jingqi organization: Key Laboratory of Forest Tree Genetics, Breeding and Cultivation of Liaoning Province, Shenyang, Liaoning, China – sequence: 5 givenname: Tianyi surname: Dong fullname: Dong, Tianyi organization: Key Laboratory of Forest Tree Genetics, Breeding and Cultivation of Liaoning Province, Shenyang, Liaoning, China – sequence: 6 givenname: Jifeng orcidid: 0000-0001-5496-5009 surname: Deng fullname: Deng, Jifeng organization: Key Laboratory of Forest Tree Genetics, Breeding and Cultivation of Liaoning Province, Shenyang, Liaoning, China – sequence: 7 givenname: Lijie surname: Zhang fullname: Zhang, Lijie organization: Key Laboratory of Forest Tree Genetics, Breeding and Cultivation of Liaoning Province, Shenyang, Liaoning, China |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36908820$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.1093/jxb/erl081 10.1016/j.scienta.2022.110885 10.13271/j.mpb.017.000396 10.3390/genes11030319 10.1007/s004290050103 10.1038/srep41124 10.1104/pp.117.1.1 10.1186/s12870-020-02372-w 10.22059/IJHST.2018.260944.249 10.1016/j.scienta.2019.109014 10.1186/s12864-017-4402-2 10.1007/BF00041177 10.1093/pcp/pce143 10.1186/s12864-018-5356-8 10.1111/j.1525-142X.2007.00182.x 10.1007/978-1-4757-9607-0_17 10.1105/tpc.3.8.771 10.1016/j.copbio.2014.11.023 10.16420/j.issn.0513-353x.2018-0023 10.1007/s11103-008-9330-8 10.1038/s41438-021-00550-x 10.15835/nbha46211183 10.1105/tpc.104.025353 10.1038/85719 10.1007/s00425-005-0086-y 10.2135/cropsci2008.03.0118 10.1590/S1516-05722009000400015 10.1007/s11703-011-1095-1 10.1023/a:1008992719010 10.1093/jxb/eraa161 10.1038/srep37306 10.1111/nph.16490 |
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Keywords | Juglans mandshurica Maxim JmLFY gene Functional verification |
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Snippet | In this study, a pBI121-
plant expression vector was constructed on the basis of obtaining the full-length sequence of the
gene from
, which was then used for... In this study, a pBI121- JmLFY plant expression vector was constructed on the basis of obtaining the full-length sequence of the JmLFY gene from Juglans... In this study, a pBI121-JmLFY plant expression vector was constructed on the basis of obtaining the full-length sequence of the JmLFY gene from Juglans... |
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SubjectTerms | Agricultural Science Arabidopsis - genetics Arabidopsis thaliana Children Cloning Flowering Flowers & plants Flowers - genetics Functional verification Gene expression Genetic aspects Genetic engineering Genetic research Genetic transformation Genetically modified plants Health aspects Infections Inflorescence - genetics JmLFY gene Juglans Juglans mandshurica Juglans mandshurica Maxim Leaves Molecular Biology Mutants Plant Breeding Plant Science Seeds Transgenic plants |
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Title | Functional verification of the JmLFY gene associated with the flowering of Juglans mandshurica Maxim |
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