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CBF在植物低温胁迫响应中的激活与调控研究进展 被引量:4
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作者 赵峻丽 陈雯 石敏 《河南农业科学》 北大核心 2020年第4期1-6,共6页
低温不仅制约植物的生长与发育,也制约植物的种植分布。为了应对低温伤害,植物通过改变基因表达和细胞内环境稳态来维持机体存活。CBF(C-repeat binding transcription factor)在植物响应低温胁迫中发挥枢纽作用,通过调控下游冷响应基因... 低温不仅制约植物的生长与发育,也制约植物的种植分布。为了应对低温伤害,植物通过改变基因表达和细胞内环境稳态来维持机体存活。CBF(C-repeat binding transcription factor)在植物响应低温胁迫中发挥枢纽作用,通过调控下游冷响应基因COR(Cold regulated)等的表达,提高植物对低温的耐受能力。对CBF的功能及其调控的下游基因、调控CBF基因的上游基因、CBF与激素互作等方面进行综述,并展望了CBF在农业生产上的应用前景,为深入研究CBF的耐冷机制奠定基础,为利用基因工程技术培育耐冷作物品种提供参考。 展开更多
关键词 cbf 低温 分子机制 ICE1 COR
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石榴低温响应因子CBF基因家族鉴定及其表达分析 被引量:8
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作者 刘龙博 郑树轩 郑洁 《西北农业学报》 CAS CSCD 北大核心 2022年第9期1154-1167,共14页
CBF(C-repeat binding factor)是AP2家族的一类转录激活因子,在植物响应低温胁迫和提高植物耐寒性方面具有重要作用。虽然多个石榴品种的基因组已经发布,但仍缺乏对其CBF基因家族的全面研究。为全面分析石榴(Punica granatum L.)CBF基... CBF(C-repeat binding factor)是AP2家族的一类转录激活因子,在植物响应低温胁迫和提高植物耐寒性方面具有重要作用。虽然多个石榴品种的基因组已经发布,但仍缺乏对其CBF基因家族的全面研究。为全面分析石榴(Punica granatum L.)CBF基因家族分子生物学特性,本文对鉴定到的PgCBFs成员进行了生物信息和表达分析。结果表明,石榴全基因组中有7个CBF基因家族成员,蛋白序列中除包含AP2结构域外,还具有CBF特征序列PKKPAGRxKFxETRHP和DSAWR;7个成员集中分布在染色体1和4上,编码蛋白质氨基酸长度为201~267aa,分子质量为21.69~29.81ku;进化分析显示PgCBFs基因家族成员分布在GroupⅡ~Ⅳ亚组中,与水稻CBF成员组成的GroupⅠ存在明显区分;除PgCBF2、PgCBF4、PgCBF5基因结构中含有1~2个内含子外,其余与其他物种类似,属内含子缺失型;编码的蛋白序列均含有保守基序Motif1~7;蛋白二级结构主要为不规则卷曲和α-螺旋,三级结构较为相似。PgCBFs基因家族扩增主要来源于串联重复,并与拟南芥、苹果、桃分别存在2对、5对和4对共线性关系;GO注释显示PgCBFs多与转录调控、低温胁迫或激素诱导相关;启动子区含有多种顺势作用元件,主要为胁迫刺激、激素诱导和光响应元件;基因表达分析发现除PgCBF6外,其余成员在根中高度表达,在低温胁迫处理下PgCBF在根和韧皮部表达量显著上调,其中PgCBF7能够快速响应并持续应答低温诱导。结合进化树、共线性、启动子以及表达分析,推测PgCBF7可能与石榴幼苗低温胁迫调控相关。本研究可为深入研究石榴CBF基因家族生物学功能提供理论基础。 展开更多
关键词 石榴(Punica granatum L.) cbf(c-repeat binding factor)基因家族 生物信息学 基因表达分析 低温胁迫 Pgcbf7
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Isolation and Expression Analysis of Two Cold-Inducible Genes Encoding Putative CBF Transcription Factors from Chinese Cabbage (Brassica pekinensis Rupr) 被引量:3
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作者 Yong Zhang Tong-Wen Yang +4 位作者 Li-Jing Zhang Teng-Guo Zhang Cui-Xia Di Shi-Jian Xu Li-Zhe An 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2006年第7期848-856,共9页
Two homologous genes of the Arabidopsis C-repeat/dehydration-responsive element binding factors (CBF/ DREB1) transcriptional activator were isolated by RT-PCR from Chinese cabbage (Brassica pekinensis Rupr. cv. Qin... Two homologous genes of the Arabidopsis C-repeat/dehydration-responsive element binding factors (CBF/ DREB1) transcriptional activator were isolated by RT-PCR from Chinese cabbage (Brassica pekinensis Rupr. cv. Qinbai 5) and were designated as BcCBF1 and BcCBF2. Each encodes a putative CBF/DREB1 protein with an AP2 (Apetal2) DNA-bindlng domain, a putative nuclear localization signal, and a possible acidic activation domain. Deduced amino acid sequences show that BcCBF1 is very similar to the Arabidopsis CBF1, whereas BcCBF2 Is different in that it contains two extra regions of 24 and 20 amino acids in the acidic domain. The mRNA accumulation profiles indicated that the expression of BcCBF1 and BcCBF2 is strongly induced by cold treatment, but does not respond similarly to dehydration or abscisic acid (ABA) treatment. However, the cold-induced accumulation of BcCBF2 mRNA was rapid but short-lived compared with that of BcCBFI. The mRNA levels of both BcCBF1 and BcCBF2 were higher in leaves than in roots when plants were exposed to cold, whereas, salt stress caused higher accumulation of BcCBF2 mRNA in roots than in leaves, suggesting that the organ specificity of the gene expression of the BcCBFs is probably stress dependent. In addition, the accumulation of BcCBF1 and BcCBF2 mRNAs was greatly enhanced by light compared with darkness when seedlings were exposed to cold. It is concluded that the two BcCBF proteins may be involved in the process of plant response to cold stress through an ABA-independent pathway and that there is also a cross-talk between the light signaling conduction pathway and the cold response pathway in B. pekinensis as in Arabidopsis. 展开更多
关键词 Brassica pekinensis cold acclimation cold induced gene c-repeat/dehydration-responsive element binding factors cbf/DREB1) expression pattern.
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Molecular Mechanism Underlying Plant Response to Cold Stress
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作者 Yiwei Cao Delight Hwarari +2 位作者 Yasmina Radani Yuanlin Guan Liming Yang 《Phyton-International Journal of Experimental Botany》 SCIE 2023年第9期2665-2682,共18页
Low temperature stress is one of the most important factors limiting plant growth and geographical distribution.In order to adapt to low temperature,plants have evolved strategies to acquire cold tolerance,known as,co... Low temperature stress is one of the most important factors limiting plant growth and geographical distribution.In order to adapt to low temperature,plants have evolved strategies to acquire cold tolerance,known as,cold acclimation.Current molecular and genomic studies have reported that annual herbaceous and perennial woody plants share similar cold acclimation mechanisms.However,woody perennials also require extra resilience to survive cold winters.Thus,trees have acquired complex dynamic processes to control the development of dormancy and cold resistance,ensuring successful tolerance during the coldest winter season.In this review,we systemically described how woody plants perceive and transduce cold stress signals through a series of physiological changes such as calcium signaling,membrane lipid,and antioxidant changes altering downstream gene expression and epigenetic modification,ultimately bud dormancy.We extended the discussion and reviewed the processes endogenous phytohormones play in regulating the cold stress.We believe that this review will aid in the comprehension of underlying mechanisms in plant acclimation to cold stress. 展开更多
关键词 Calcium signaling cold stress c-repeat binding factor(cbf) DORMANCY plants
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不同细胞类型对cbf α1调控DSPP基因转录的影响 被引量:1
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作者 郭婷 曹罡 +2 位作者 余擎 肖明振 赵守亮 《临床口腔医学杂志》 2007年第5期272-274,共3页
目的:观察核心结合因子α1(core binding factor α1,cbf α1)对不同细胞中牙本质涎磷蛋白(dentin sialophosphoprotein,DSPP)基因转录调控的影响。方法:选择Hela和小鼠成牙本质细胞样细胞MDPC-23为实验细胞;DSPP基因上游2.6kb片段为启... 目的:观察核心结合因子α1(core binding factor α1,cbf α1)对不同细胞中牙本质涎磷蛋白(dentin sialophosphoprotein,DSPP)基因转录调控的影响。方法:选择Hela和小鼠成牙本质细胞样细胞MDPC-23为实验细胞;DSPP基因上游2.6kb片段为启动子。采用瞬时转染、报告基因等方法观察在两种细胞中,cbf α1对DSPP基因启动子启动活性的影响。结果:在MDPC-23及Hela细胞中,pGL3-Enhancer-2.6K与pcDNA3-cbf α1共转染组荧光素酶的表达量均小于pGL3-Enhancer-2.6K与pcDNA3共转染组(P<0.01);在MDPC-23细胞中变化更为明显。结论:cbf α1对DSPP基因的转录调控作用受细胞类型的影响。 展开更多
关键词 核心结合因子Α1 瞬时转染 报告基因 转录调控
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