Article(id=1322924403503280843, tenantId=1146029695717560320, journalId=1322258771877134531, issueId=1322924314793750542, articleNumber=null, orderNo=null, doi=10.14067/j.cnki.1673-923x.2026.10.018, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=1757865600000, receivedDateStr=2025-09-15, revisedDate=1767110400000, revisedDateStr=2025-12-31, acceptedDate=null, acceptedDateStr=null, onlineDate=1793339356541, onlineDateStr=2026-10-30, pubDate=1792857600000, pubDateStr=2026-10-25, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793339356541, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793339356541, creator=13701087609, updateTime=1793339356541, updator=13701087609, issue=Issue{id=1322924314793750542, tenantId=1146029695717560320, journalId=1322258771877134531, year='2026', volume='46', issue='10', pageStart='1', pageEnd='256', issueExtLink='null', onlineDate='null', pubDate='1792857600000', pubDateStr='2026-10-25', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=1, specialIssue=null, createTime=1793339335392, creator='13701087609', updateTime=1793344604640, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322946415693017274, tenantId=1146029695717560320, journalId=1322258771877134531, issueId=1322924314793750542, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322946415693017275, tenantId=1146029695717560320, journalId=1322258771877134531, issueId=1322924314793750542, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=200, endPage=209, ext={EN=ArticleExt(id=1322924403687830221, articleId=1322924403503280843, tenantId=1146029695717560320, journalId=1322258771877134531, language=EN, title=Cloning and drought resistance function of BpbZIP36 gene in Betula platyphylla, columnId=null, journalTitle=Journal of Central South University of Forestry & Technology, columnName=null, runingTitle=null, highlight=null, articleAbstract=
【Objective】

By cloning the BpbZIP36 gene, constructing a plant expression vector, and obtaining stable transgenic birch plants, this study aimed to investigate the drought resistance function of the BpbZIP36 gene.

【Method】

Using birch as the experimental material, the BpbZIP36 gene was cloned from birch cDNA as the template. Bioinformatics analysis was performed on the gene, and the pROK2-BpbZIP36 plant expression vector was constructed and introduced into birch seedlings to obtain transgenic birch overexpressing BpbZIP36. The transgenic birch plants and wild-type were subjected to drought stress to study the drought resistance function of the BpbZIP36 gene.

【Result】

A bZIP gene was obtained from the birch genome database, with an open reading frame (ORF) of 1 269 bp encoding 422 amino acids. The results of multiple sequence alignment showed that the BpbZIP36 protein was similar to the bZIP protein of other plants and a conserved bZIP structural domain. qRT-PCR results showed that the BpbZIP36 gene was expressed in roots, stems, and leaves. In stems and leaves, the expression level of BpbZIP36 peaked at 72 h, while in roots, the highest expression was observed at 24 h of stress treatment, indicating that the BpbZIP36 gene could be induced by drought stress. Physiological index and histochemical staining analyses revealed that under drought stress, the transgenic birch overexpressing BpbZIP36 exhibited lower MDA, H2O2 content, and relative electrical conductivity compared to wild-type plants, indicating better cell membrane integrity. The SOD, POD and CAT activities, as well as relative water content, were higher in the transgenic birch. DAB staining showed the lightest coloration in the three overexpression lines, suggesting lower H2O2 accumulation and reduced cellular damage. These results demonstrated that the drought resistance capacity of the transgenic birch overexpressing BpbZIP36 was stronger than that of wild-type.

【Conclusion】

Overexpression of the BpbZIP36 gene enhances the drought resistance capability of transgenic birch.

, authors=Yanmin Wang1, 2, 3, Mingyue Xiang1, Jing Li3, Zhihui Yin3, Zhenghua Li3, Chengbo Guo3, Caiqiu Gao1, Hui Bai3, Haixia Li3, authorsList=Yanmin Wang, Mingyue Xiang, Jing Li, Zhihui Yin, Zhenghua Li, Chengbo Guo, Caiqiu Gao, Hui Bai, Haixia Li, authorCompany=null, correspAuthors=Hui Bai, Haixia Li, authorNote=null, correspAuthorsNote=null, copyrightStatement=© 2026 Journal of Central South University of Forestry & Technology, copyrightOwner=Journal of Central South University of Forestry & Technology, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1322924404027568847, articleId=1322924403503280843, tenantId=1146029695717560320, journalId=1322258771877134531, language=CN, title=白桦BpbZIP36基因克隆及抗旱功能, columnId=1322924272984929210, journalTitle=中南林业科技大学学报, columnName=生物学, runingTitle=null, highlight=null, articleAbstract=
【目的】

通过克隆BpbZIP36基因构建植物表达载体,获得稳定转化白桦转基因植株,对转基因株系进行干旱胁迫,探究BpbZIP36基因的抗旱功能。

【方法】

以白桦cDNA为模板克隆BpbZIP36基因,对测序获得的BpbZIP36基因序列进行生物信息学分析,构建pROK2-BpbZIP36植物表达载体后转入白桦苗中,得到稳定转化转BpbZIP36基因白桦,对转BpbZIP36基因过表达白桦植株及对照进行干旱胁迫,研究BpbZIP36基因的抗旱功能。

【结果】

从白桦基因组数据库中获得一条bZIP基因,开放读码框全长1 269 bp,编码422个氨基酸。多序列结果显示,白桦bZIP36蛋白与其他各植物中bZIP蛋白具有相似性,都具有保守的bZIP结构域。qRT-PCR研究结果显示,BpbZIP36基因在根、茎、叶中均有表达,在茎和叶中,BpbZIP36基因的表达量在胁迫72 h时达到峰值,而在根中胁迫处理24 h时表达量最高,表明BpbZIP36基因能够被干旱胁迫诱导表达。对转基因白桦植株进行干旱胁迫后,生理指标和组织化学染色分析结果显示:干旱胁迫条件下3个过表达白桦株系的MDA、H2O2含量和相对电导率低于野生型,细胞膜完整性较好;过表达白桦的SOD、POD、CAT活性、相对含水量高于野生型,在过表达的3个株系中DAB染色棕色斑点少、着色轻,说明过表达的3个株系中H2O2含量较少,继而反映出细胞受损程度低,过表达白桦抗旱能力强于野生型白桦。

【结论】

BpbZIP36基因过表达能够提高转基因白桦的抗旱能力。

, authors=王艳敏1, 2, 3, 项明月1, 李静3, 殷志辉3, 李正华3, 郭成博3, 高彩球1, 白卉3, 李海霞3, authorsList=王艳敏, 项明月, 李静, 殷志辉, 李正华, 郭成博, 高彩球, 白卉, 李海霞, authorCompany=null, correspAuthors=白卉, 李海霞, authorNote=

王艳敏(),研究员,博士。

, correspAuthorsNote=
白卉(),研究员,博士。
李海霞(),副研究员,硕士。
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2.Forestry Research Academy of Heilongjiang Province, Harbin 150081, Heilongjiang, China
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白桦BpbZIP36基因克隆及抗旱功能
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王艳敏 1, 2, 3 , 项明月 1 , 李静 3 , 殷志辉 3 , 李正华 3 , 郭成博 3 , 高彩球 1 , 白卉 3 , 李海霞 3
中南林业科技大学学报 | 生物学 2026,46(10): 200-209
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中南林业科技大学学报 |生物学 2026 , 46 (10) : 200 -209
白桦BpbZIP36基因克隆及抗旱功能
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王艳敏1, 2, 3 , 项明月1, 李静3, 殷志辉3, 李正华3, 郭成博3, 高彩球1, 白卉3 , 李海霞3
作者信息
  • 1.东北林业大学 a. 林学院;b. 林木遗传育种全国重点实验室,黑龙江 哈尔滨 150040
  • 2.黑龙江省林业科学院 黑龙江 哈尔滨 150081
  • 3.黑龙江省林业科学研究所 黑龙江省速生林木培育重点实验室,黑龙江 哈尔滨 150081
通讯作者:
白卉(),研究员,博士。
李海霞(),副研究员,硕士。
作者简介:

王艳敏(),研究员,博士。

Cloning and drought resistance function of BpbZIP36 gene in Betula platyphylla
Yanmin Wang1, 2, 3 , Mingyue Xiang1, Jing Li3, Zhihui Yin3, Zhenghua Li3, Chengbo Guo3, Caiqiu Gao1, Hui Bai3 , Haixia Li3
Affiliations
  • 1.a. College of Forestry; b. State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin 150040, Heilongjiang, China
  • 2.Forestry Research Academy of Heilongjiang Province, Harbin 150081, Heilongjiang, China
  • 3.Forest Research Institute of Heilongjiang Province, Key Laboratory of Fast-Growing Tree Cultivating of Heilongjiang Province, Harbin 150081, Heilongjiang, China
出版时间: 2026-10-25 doi: 10.14067/j.cnki.1673-923x.2026.10.018
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【目的】

通过克隆BpbZIP36基因构建植物表达载体,获得稳定转化白桦转基因植株,对转基因株系进行干旱胁迫,探究BpbZIP36基因的抗旱功能。

【方法】

以白桦cDNA为模板克隆BpbZIP36基因,对测序获得的BpbZIP36基因序列进行生物信息学分析,构建pROK2-BpbZIP36植物表达载体后转入白桦苗中,得到稳定转化转BpbZIP36基因白桦,对转BpbZIP36基因过表达白桦植株及对照进行干旱胁迫,研究BpbZIP36基因的抗旱功能。

【结果】

从白桦基因组数据库中获得一条bZIP基因,开放读码框全长1 269 bp,编码422个氨基酸。多序列结果显示,白桦bZIP36蛋白与其他各植物中bZIP蛋白具有相似性,都具有保守的bZIP结构域。qRT-PCR研究结果显示,BpbZIP36基因在根、茎、叶中均有表达,在茎和叶中,BpbZIP36基因的表达量在胁迫72 h时达到峰值,而在根中胁迫处理24 h时表达量最高,表明BpbZIP36基因能够被干旱胁迫诱导表达。对转基因白桦植株进行干旱胁迫后,生理指标和组织化学染色分析结果显示:干旱胁迫条件下3个过表达白桦株系的MDA、H2O2含量和相对电导率低于野生型,细胞膜完整性较好;过表达白桦的SOD、POD、CAT活性、相对含水量高于野生型,在过表达的3个株系中DAB染色棕色斑点少、着色轻,说明过表达的3个株系中H2O2含量较少,继而反映出细胞受损程度低,过表达白桦抗旱能力强于野生型白桦。

【结论】

BpbZIP36基因过表达能够提高转基因白桦的抗旱能力。

白桦  /  BpbZIP36基因  /  基因克隆  /  抗旱功能
【Objective】

By cloning the BpbZIP36 gene, constructing a plant expression vector, and obtaining stable transgenic birch plants, this study aimed to investigate the drought resistance function of the BpbZIP36 gene.

【Method】

Using birch as the experimental material, the BpbZIP36 gene was cloned from birch cDNA as the template. Bioinformatics analysis was performed on the gene, and the pROK2-BpbZIP36 plant expression vector was constructed and introduced into birch seedlings to obtain transgenic birch overexpressing BpbZIP36. The transgenic birch plants and wild-type were subjected to drought stress to study the drought resistance function of the BpbZIP36 gene.

【Result】

A bZIP gene was obtained from the birch genome database, with an open reading frame (ORF) of 1 269 bp encoding 422 amino acids. The results of multiple sequence alignment showed that the BpbZIP36 protein was similar to the bZIP protein of other plants and a conserved bZIP structural domain. qRT-PCR results showed that the BpbZIP36 gene was expressed in roots, stems, and leaves. In stems and leaves, the expression level of BpbZIP36 peaked at 72 h, while in roots, the highest expression was observed at 24 h of stress treatment, indicating that the BpbZIP36 gene could be induced by drought stress. Physiological index and histochemical staining analyses revealed that under drought stress, the transgenic birch overexpressing BpbZIP36 exhibited lower MDA, H2O2 content, and relative electrical conductivity compared to wild-type plants, indicating better cell membrane integrity. The SOD, POD and CAT activities, as well as relative water content, were higher in the transgenic birch. DAB staining showed the lightest coloration in the three overexpression lines, suggesting lower H2O2 accumulation and reduced cellular damage. These results demonstrated that the drought resistance capacity of the transgenic birch overexpressing BpbZIP36 was stronger than that of wild-type.

【Conclusion】

Overexpression of the BpbZIP36 gene enhances the drought resistance capability of transgenic birch.

Betula platyphylla  /  BpbZIP36 gene  /  gene cloning  /  drought-resistance function
王艳敏, 项明月, 李静, 殷志辉, 李正华, 郭成博, 高彩球, 白卉, 李海霞. 白桦BpbZIP36基因克隆及抗旱功能. 中南林业科技大学学报, 2026 , 46 (10) : 200 -209 . DOI: 10.14067/j.cnki.1673-923x.2026.10.018
Yanmin Wang, Mingyue Xiang, Jing Li, Zhihui Yin, Zhenghua Li, Chengbo Guo, Caiqiu Gao, Hui Bai, Haixia Li. Cloning and drought resistance function of BpbZIP36 gene in Betula platyphylla[J]. Journal of Central South University of Forestry & Technology, 2026 , 46 (10) : 200 -209 . DOI: 10.14067/j.cnki.1673-923x.2026.10.018
  • 黑龙江省自然科学基金资助项目(LH2023C104)
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2026年第46卷第10期
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doi: 10.14067/j.cnki.1673-923x.2026.10.018
  • 接收时间:2025-09-15
  • 首发时间:2026-10-30
  • 出版时间:2026-10-25
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  • 收稿日期:2025-09-15
  • 修回日期:2025-12-31
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黑龙江省自然科学基金资助项目(LH2023C104)
作者信息
    1.东北林业大学 a. 林学院;b. 林木遗传育种全国重点实验室,黑龙江 哈尔滨 150040
    2.黑龙江省林业科学院 黑龙江 哈尔滨 150081
    3.黑龙江省林业科学研究所 黑龙江省速生林木培育重点实验室,黑龙江 哈尔滨 150081

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白卉(),研究员,博士。
李海霞(),副研究员,硕士。
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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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