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1、参与原核生物参与原核生物DNADNA复制的复制的酶类和蛋白质酶类和蛋白质Enzymes and Proteins Involved in DNA Enzymes and Proteins Involved in DNA Replication in ProkaryotesReplication in Prokaryotes 高方远高方远 马欣荣马欣荣 康海岐康海岐DNAreplication(bacteria)InitiationElongationTerminationDaughterDNApartition*theoriginofreplicationisdefined *replicat
2、ionbubble. *Replicationfork*Unidirectionalorbidirectional.OriginsFigure13.9Theleadingstrandissynthesizedcontinuouslywhilethelaggingstrandissynthesizeddiscontinuously.Elongation(semidiscontinuous)termination参与参与DNA复制的酶类复制的酶类1 1、DNADNA聚合酶聚合酶2 2、DNADNA引发酶（引发酶（DNADNA primase primase）3 3、DNADNA连接酶连接酶4 4、
3、与、与DNADNA几何学性质相关的酶几何学性质相关的酶 IpolAmajorrepairenzymeIIpolBminorrepairenzymeIIIpolCreplicaseIVdinBSOSrepairVumuC、DSOSrepairDNApolymerasesinE.coliDNAPolymeraseIDNApolymerase35exonuclease53exonucleaseFigure 13.8 The catalytic domain of a DNA polymerase has a DNA-binding cleft created by three subdomains.
4、 The active site is in the palm. Proofreading is provided by a separate active site in an exonuclease domain. Figure13.7CrystalstructureofphageT7DNApolymerasehasarighthandstructure.DNAliesacrossthepalmandisheldbythefingersandthumb.PhotographkindlyprovidedbyCharlesRichardsonandTomEllenberger.Figure13
5、.5Nicktranslationreplacespartofapre-existingstrandofduplexDNAwithnewlysynthesizedmaterial.DNAPolymeraseISubunitcompositionofE.coli DNApolymeraseIIIholoenzymesubunitmolecularmassfunctionsubassemblies(KDa)129.9DNApolymerase27.535exonucleasecore8.6stimulatesexonuclease71.1dimerizescorePolIIIbindscomple
6、x47.5bindsATP38.7bindstoPolIII36.9bindstoandcomplex16.6bindstoSSBDNA-dependent15.2bindstoandATPase40.6slidingclampE.coliPolIIIBeta-subunitFigure13.18DNApolymeraseIIIholoenzymeassemblesinstages,generatinganenzymecomplexthatsynthesizestheDNAofbothnewstrands.Fig.1.ModelofSOStranslesionreplicationbyDNAp
7、olymeraseV.ThetwoDNAstrandsareshownasgreen lines,andthereplication-blockinglesionisrepresentedbythered rectangle.ThethreemajorstepsinTLRarepre-initiation(2),inwhichtheRecAnucleoproteinfilamentsassembles;initiation(3and4),whichinvolvesbindingofpolVtotheprimer-templateandloadingofthesubunitclamp;andle
8、sion bypassbypolVholoenzyme(5).SSBissuggestedtohelpindisplacingRecAfromDNAbothattheinitiationandlesionbypasssteps. E. coli DNA polymerase IV（dinBgene） * dinBdinB 基基因的表达需要因的表达需要 DNADNA损伤诱导损伤诱导 * * 与与UmuCUmuC、 UmuDUmuD同属同属Y Y 家族家族DNADNA聚合酶聚合酶 * E.coliDNApolymeraseIV无校正功能，易于延长一些凸无校正功能，易于延长一些凸出的引物或模板结构。
9、出的引物或模板结构。2 2、DNADNA引发酶（引发酶（DNADNA primase primase）UsehostRNApolymeraseasprimase(M13)primosomeprimase(dnaGprotein)(E.coli)otherproteinsX174:onlyprimase,withouttheotherproteinsInitiationrequiresseveralenzymaticactivities,includinghelicases,single-strandbindingproteins,andsynthesisoftheprimer.Adenovir
10、usterminalproteinbindstothe5 endofDNAandprovidesaC-OHendtoprimesynthesisofanewDNAstrand.AprimerterminusisgeneratedwithinduplexDNA.Nicktranslationreplacespartofapre-existingstrandofduplexDNAwithnewlysynthesizedmaterial.DNAPolymeraseI与与DNADNA几何学性质相关的酶几何学性质相关的酶解旋酶解旋酶（Helicase）拓扑异构酶拓扑异构酶（Topoisomerases）
11、解旋酶解旋酶（Helicase）至少至少4 4种种helicaseshelicases * * reprep helicasehelicase * DNA * DNA helicase helicase IIII * DNA * DNA helicasehelicase III III * * dnaBdnaB Protein: Protein: 在在E.E.colicoli DNA DNA复制中解开复制中解开 DNADNA双链双链拓扑异构酶拓扑异构酶（Topoisomerases）拓扑异构酶拓扑异构酶I(topAgene)actonhighlynegativelysupercoiledDNA
12、stabilizesingle-strandedregionsFigure14.16BacterialtypeItopoisomerasesrecognizepartiallyunwoundsegmentsofDNAandpassonestrandthroughabreakmadeintheother.拓扑异构酶拓扑异构酶IIII TypeIItopoisomerasesgenerallyrelaxbothnegativeandpositivesupercoils.ThereactionrequiresATPFigure14.17TypeIItopoisomerasescanpassadupl
13、exDNAthroughadouble-strandbreakinanotherduplex.拓扑异构酶拓扑异构酶IVIV与与子代子代DNADNA分子的分开有关分子的分开有关参与参与DNA复制的蛋白质复制的蛋白质1 1、参与复制起始的蛋白质因子参与复制起始的蛋白质因子Originalcomplx: DnaA、DnaB、DnaC、DnaG、HUandSSB Theminimaloriginisdefinedbythedistancebetweentheoutsidemembersofthe13-merand9-merrepeats Prepriminginvolvesformationofaco
14、mplexbysequentialassociationofproteins,leadingtotheseparationofDNAstrands.methylationattheoriginAmembrane-boundinhibitorbindstohemimethylatedDNAattheorigin,andmayfunctionbypreventingthebindingofDnaA.ItisreleasedwhentheDNAisremethylated.SeqAThecomplexatoriCcanbedetectedbyelectronmicroscopy. Antibodie
15、sofdnaAproteinHUThe protein HU is a general DNA-binding protein in E. coli . Its presence is not absolutely required to initiate replication in vitro, but it stimulates the reaction. HU has the capacity to bend DNA, and is likely to be involved in some general structural capacity. 2 2、参与复制延伸的蛋白质因子、参
16、与复制延伸的蛋白质因子(DnaG)(DnaB)2 2、参与参与复制复制终止终止的蛋的蛋白质白质因子因子TusHow do the daughter DNAs become disentangled? 与真核生物不同，细菌的与真核生物不同，细菌的DNADNA复制复制、染色体重染色体重新折叠以及姊妹染色体的分开新折叠以及姊妹染色体的分开是同时发生的。是同时发生的。 细菌中姊妹染色体的分开的机制与真核生物不细菌中姊妹染色体的分开的机制与真核生物不同。细菌染色体的同。细菌染色体的DNADNA分子本身卷入了分开机制。分子本身卷入了分开机制。 细菌的多复制叉复制（细菌的多复制叉复制（multiple mu
17、ltiple replicationreplication）与真核生物的复制方式不同。与真核生物的复制方式不同。 * * 多拷贝的多拷贝的oriCoriC * * 只有一个终止序列只有一个终止序列Asimplifiedmodelofthebacterialcellcycle.Themodelissimplifiedtoignoremultiforkreplication.SMC类似物类似物A model of a circular chromosome that is undergoing multifork replication in a rod-shaped bacterium. 复制起
18、点及终点在细胞中的位置复制起点及终点在细胞中的位置1 1、膜片段中有复制起始区与终止区的富集推断锚定、膜片段中有复制起始区与终止区的富集推断锚定蛋白在定位中的作用。蛋白在定位中的作用。SeqA2 2、位于中间位置、位于中间位置 复制工厂复制工厂 的动力作用的动力作用 多蛋白复合体：多蛋白复合体：polymerasepolymerase, , helicase helicase and and accociated accociated proteinsproteins 特殊蛋白质（特殊蛋白质（PolCPolC-GFP-GFP、SeqASeqA) ) 的定位；的定位；H3H3同位素标记；同位素标
19、记； pull DNA templatepull DNA template duplicated duplicated release DNA outward during replication release DNA outward during replicationTheextrusion-capturemodelforbacterialchromosomepartitioning.3 3、与染色体组织（、与染色体组织（organizationorganization）、）、紧结紧结( (compactioncompaction) )和超螺旋和超螺旋( (helicasehelicas
20、e) )有关的蛋白质作用有关的蛋白质作用 SMCSMC MukBMukB to organize the chromosome into a higherto organize the chromosome into a higher order structure by constraining order structure by constraining supercoilssupercoils.(.(causecause) ) PartitioningMotorprotein(altered)Chromosomepartitioning(consequence)HU;Hbsu;Term
21、inus-specificchromosomepartitioningevents. Tyrosinesite-specificrecombinasesE.coliCodV,RipXB.subtilisPost-septationpartitioningFtsKPBP2RodAPBP3peptidoglycan(肽聚糖肽聚糖)EnvAFigure12.27Failureofcelldivisiongeneratesmultinucleatedfilaments.E. coligenerateanucleatecellswhenchromosomesegregationfails.Cellswi
22、thchromosomesstainblue;daughtercellslackingchromosomeshavenobluestain.ThisfieldshowscellsofthemukBmutant;bothnormalandabnormaldivisionscanbeseen.PhotographkindlyprovidedbySotaHiraga. Minicells:anucleatecellsProblem1.1.哪些哪些DNADNA位点和蛋白质对复制起点的移动及定位起决定性作位点和蛋白质对复制起点的移动及定位起决定性作用？用？2.2.这些位点和蛋白质在指数生长期和进入静止期是否相同？这些位点和蛋白质在指数生长期和进入静止期是否相同？3.3.细胞分裂后，终止序列是怎样定位到细胞的中央部位的？细胞分裂后，终止序列是怎样定位到细胞的中央部位的？4.4.能够进行多复制叉复制的细菌与不能进行多复制叉复制的细能够进行多复制叉复制的细菌与不能进行多复制叉复制的细菌在染色体分开机制上有什么不同？菌在染色体分开机制上有什么不同？5.5.不同物理形状的染色体分开时有差异吗？不同物理形状的染色体分开时有差异吗？20.
