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桉树焦枯病是由丽赤壳属(Calonectria spp.)真菌引起的世界性病害,主要发生在桉树幼苗和4年生以下的人工幼林[1-2]。该病原菌可侵染桉树幼茎、叶片、枝杆、树梢等多个部位,使苗木猝倒、根腐,叶片焦枯、卷曲脱落,枝条枯死,造成桉苗腐烂病以及生长后期的焦枯、顶枯、叶枯病。在我国广东、广西、海南、福建、台湾等桉树苗圃和人工林都有不同程度的发生,每次病害流行均导致大面积桉树林枯萎死亡,造成桉树人工林生产量明显下降[3-4]。据估计,福建省因该病害造成的年经济损失达0.518亿元[5]。桉树具有丰富的遗传资源,不同品系对焦枯病菌的抗性存在明显差异[6-8]。
苯丙烷代谢途径是植物体中一条重要的代谢途径[9-10]。苯丙氨酸解氨酶(PAL)是苯丙烷类代谢的关键酶和限速酶,主要负责催化L-苯丙氨酸脱氨形成反式肉桂酸,后者是植物合成木质素、植保素、黄酮、类黄酮等多种酚类次级代谢产物的前体物质,这些次级产物在调节植物生长发育及提高抗逆性中起着重要作用。目前,已从植物中克隆到多个PAL基因并研究了相应功能[11-12]。大多数植物PAL基因的编码序列长度约为2 100 bp,包含2个外显子和1个内含子,其中,外显子长度分别约为400、1 700 bp,内含子的位置相对保守,但长度差异很大。植物PAL蛋白一般含有PAL-HAL、PLN02457及phe_am_lyase三个保守结构域,其中,酶活性位点在PAL-HAL结构域上。植物PAL活性与其抗病性密切相关[13],在病原物侵染后,PAL活性往往呈现出先升高后下降的趋势,且抗病品系PAL活性高于感病品系[14]。水稻感染稻瘟病、小麦感染白粉病和赤霉病、玉米感染黑穗病、锥栗感染疫病后的PAL活性均出现上述变化趋势[15-19]。桉树PAL基因较少研究,PAL基因对桉树抗焦枯病菌的作用也未见报道。本研究从尾细桉M1基因组中克隆到1个PAL基因,并进行了生物信息学分析,探讨了接种Ca. pseudoreteaudii后不同品系PAL基因的表达特征,为进一步研究PAL基因在桉树抵抗焦枯病菌侵染的作用机制奠定基础。
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抗病品系尾细桉M1(Eucalyptus urophylla × E. tereticornis M1)和中感品系尾巨桉3229号(E. urophylla × E. grandis 3229)、感病品系巨桉5号(E. grandis 5)扦插苗及桉树焦枯病菌(Calonectria pseudoreteaudii YA51)由福建农林大学森林保护研究所提供[6]。质粒pDoner207由福建农林大学功能基因组研究中心惠赠。孢子悬浮液的配制参照Feng等[20]的方法。
将15棵桉树扦插苗(苗龄3个月,苗高25 cm)栽植于带土花盆,并置于人工气候箱(昼夜温度分别为25℃和23℃,相对湿度90%,光暗时间比14/10)中适应性培养7 d后,用75%酒精消毒,再用ddH2O冲洗23遍,将浓度为2.0×105 个·mL-1的分生孢子悬浮液均匀地喷洒于植株上,再置于人工气候箱保湿培养。分别于接种后0、12、24、48、72 h采集叶片,每个时间点从不同幼苗上采集的叶片混合在一起,液氮速冻后-80℃冰箱保存备用。
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按照Plant Genomic DNA Kit(TIANGEN)的说明书提取尾细桉M1的基因组DNA。
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采用改良CTAB法提取桉树总RNA [21]。检测合格后,以总RNA为模板,按照ScriptTM RT reagent Kit with gDNA Eraser (TaKaRa)说明书合成cDNA,置于-20℃备用。
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根据巨桉(E. grandis)PAL基因(Eucgr.J01079.1)cDNA序列在其可能的开放阅读框两端设计引物(表 1)。以尾细桉M1的基因组DNA为模板,分两段克隆PAL基因。反应程序:95℃预变性3 min;95℃变性15 s,60℃退火15 s,72℃延伸1 min,30个循环;72℃保温5 min,4℃保存。琼脂糖凝胶电泳检测PCR产物,并回收目的片段。采用重叠延伸扩增技术(SOE)连接两个目的片段。第一步反应体系:10× LA Buffer 5 μL,dNTP mix 2 μL,Templax 1 1 μL,Templax 2 0.5 μL,LA Tag 0.25 μL,ddH2O补足48 μL,反应程序:95℃预变性3 min;94℃变性30 s,64℃退火1 min,72℃延伸1 min,10个循环;72℃保温7 min,4℃保存。第二步反应体系:第一步反应产物48 μL,引物F1 1 μL,R2 1 μL,反应条件:94℃预变性4 min;94℃变性40 s,60℃退火40 s,72℃延伸2 min,30个循环;72℃保温7 min,4℃保存。电泳检测目的条带,回收纯化后连接到pDoner207,并用Gateway技术进行BP反应,转化DH5α感受态细胞,菌液PCR鉴定为阳性克隆后,送至上海华大基因生物技术有限公司测序。
表 1 基因克隆及荧光定量PCR引物
Table 1. Primers used for cloning and real-time PCR
基因名称
Gene name用途
Function序列
Primer sequence (5’-3’)片段长度
Length of fragment/bpPAL Clone F1:ATGGAGATGGAGAGCACC
R1:CTTATAAGTTCCTTCTGCAAAG398 PAL Clone F2:TTGCAGAAGGAACTTATAAGGTTCTTGAATGCCGGGAT
R2:CTAAGAGATGGGAAGAGGAG1 750 PAL RT-PCR F3:TCGAGTCCAGTACGAGACAGG
R3:CTAAGAGATGGGAAGAGGAGCAC241 Actin RT-PCR F:TTCTACTATGTTCCCAGGTATCGC
R:GACCAGATTCATCATACTCACCCT194 -
利用ORF finder预测基因的开放阅读框(ORF)和编码序列;采用NCBI的Blast工具分析核苷酸和氨基酸序列相似性;利用ProtParam(http://expasy.org/tools/protparam.html)在线分析氨基酸序列的理化性质;采用ProtScale分析蛋白质的疏水性/亲水性;采用NetPhos分析蛋白的磷酸化位点;利用SOPMA分析蛋白的二级结构;利用MEGA7.0软件及邻接(NJ)法构建进化树。
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以Actin(Eucgr.I00241.1)为内参基因,根据SYBR Premix Ex TaqTM(Tli RNaseH Plus)(TaKaRa)的操作说明,在荧光定量PCR仪(Eppendorf)上分析不同桉树品系PAL基因在焦枯病菌胁迫下的表达情况。反应体系:1 μL cDNA,0.3 μL F3,0.3 μL R3,5 μL SYBR Premix ExTaq,ddH2O补足10 μL。反应条件:95℃ 2 min;95℃ 30 s,60℃ 15 s,68℃ 20 s,40 cycles。每个样品技术重复3次,以0 h为对照,以2-△△CT方法分析相对表达量。
桉树PAL基因克隆及焦枯病菌诱导下的表达分析
Cloning of PAL Gene from Eucalyptus and Its Expression under Calonectria pseudoreteaudii Stress
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摘要:
目的 克隆桉树苯丙氨酸解氨酶基因(PAL),分析其序列特征及在焦枯病菌诱导下的表达特征,为探究桉树抗焦枯病机理提供理论支撑。 方法 通过SOE-PCR技术从尾细桉M1中克隆PAL基因,利用real-time PCR分析其在焦枯病菌诱导下的表达特性。 结果 克隆得到尾细桉M1 PAL基因,其ORF序列长2 142 bp,编码713个氨基酸,与其他已发表的桉树PAL相似性均在99%以上。序列分析发现,其编码蛋白是一类稳定的亲水性蛋白,含有丝氨酸、苏氨酸和酪氨酸3个磷酸化位点,二级结构以α-螺旋和β-折叠为主,具有典型的苯丙氨酸和组氨酸解氨酶保守结构域。进一步分析桉树不同品系PAL基因的表达趋势,结果发现,不同品系PAL基因在焦枯病菌诱导下均表现为明显的上调表达,且抗性越强,PAL基因越早上调,上调表达量越大。 结论 从尾细桉M1中克隆得到的PAL基因具有典型的PAL家族成员特征,推测该基因可能通过参与酚类防御性物质或者信号分子SA等物质的合成,进而在桉树抵抗焦枯病菌侵染的过程中发挥重要作用。 Abstract:Objective This study aimed at cloning the cDNA sequence of Eucalyptus phenylalanin ammonia-lyase (PAL) gene, analyzing its characteristics, and investigating its expressions in Eucalyptus under the infection of Calonectria pseudoreteaudii. Method SOE-PCR technology was used to clone PAL gene from E. urophylla×E. tereticornis M1. The expression level of PAL gene in different Eucalyptus cultivars infected with C. pseudoreteaudii were analyzed by RT-PCR. Result One PAL gene was cloned. Its ORF sequence was 2 142 bp, and encoded 713 amino acids, which showed high similarity to the PAL from other Eucalyptus, with 99% identity. Amino acids sequence analysis indicated that the predicted PAL protein was a stable hydrophilic protein, including three phosphorylation sites (serine, threonine and tyrosine). Its secondary structure was rich in α-helix and random coil. The predicted protein contained phenylalanine and histidine ammonia-lyase conserved structure. The results showed that the PAL gene was significantly up-regulated in all tested cultivars. Moreover, the PAL gene was earlier and more significantly up-regulated in the stronger resistant cultivars. Conclusion The PAL gene which was cloned from E. urophylla×E. tereticornis M1 has typical characteristics of PAL family. It is speculated that PAL gene may participant in the synthesis of phenolic compounds or signal molecule salicylic acid, then improves the resistance of Eucalyptus to C. pseudoreteaudii. -
Key words:
- Eucalyptus
- / phenylalanine ammonia-lyase
- / SOE-PCR
- / bioinformatics
- / Calonectria pseudoreteaudii
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表 1 基因克隆及荧光定量PCR引物
Table 1. Primers used for cloning and real-time PCR
基因名称
Gene name用途
Function序列
Primer sequence (5’-3’)片段长度
Length of fragment/bpPAL Clone F1:ATGGAGATGGAGAGCACC
R1:CTTATAAGTTCCTTCTGCAAAG398 PAL Clone F2:TTGCAGAAGGAACTTATAAGGTTCTTGAATGCCGGGAT
R2:CTAAGAGATGGGAAGAGGAG1 750 PAL RT-PCR F3:TCGAGTCCAGTACGAGACAGG
R3:CTAAGAGATGGGAAGAGGAGCAC241 Actin RT-PCR F:TTCTACTATGTTCCCAGGTATCGC
R:GACCAGATTCATCATACTCACCCT194 -
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