遗传学名词解释
遗传学名词解释

遗传学名词解释1、遗传(heredity):一种生物只能繁衍同种生物,世代间相似的现象就是遗传。
2、变异(variation):亲代和子代之间、子代和子代之间相似而不完全相同,这种生物个体间的差异叫变异。
3、遗传学(Genetics):是研究生物的遗传与变异规律的一门生物学分支科学;是研究遗传信息传递与表达的一门生物学分支科学。
4、基因(gene):孟德尔遗传分析中指的遗传因子。
基因位于染色体上,是具有特定核苷酸顺序的片段,是储存遗传信息的功能单位。
5、基因座(locus):基因在染色体上所处的位置。
6、等位基因(alleles):在同源染色体上占据相同座位的两个不同形式的基因,是由突变所造成的许多可能的状态之一。
7、显性基因(dominant):在杂合状态中,能够表现其表型效应的基因,一般以大写字母表示。
8、隐性基因(recessive):在杂合状态中,不表现其表型效应的基因,一般以小写字母表示。
9、基因型(genotype):个体或细胞的特定基因的组成。
10、表型(phenotype):生物体某特定基因所表现的性状(可以观察到的各种形体特征、基因的化学产物、各种行为特性等)。
11、纯合体(homozygote):基因座上有两个相同的等位基因,就这个基因座而言,这种个体或细胞称为纯合体。
12、杂合体(hoterozygote):基因座上有两个不同的等位基因。
13、真实遗传(true breeding):子代性状永远与亲代性状相同的遗传方式。
14、回交(backcross):杂交产生的子一代个体再与其亲本进行交配的方式。
15、测交(testcross):杂交产生的子一代个体再与其隐性(或双隐性)亲本进行交配的方式,用以测验子代个体的基因型的一种回交。
16、性状:在遗传学研究中通常把生物个体的形态、结构、生理生化等特性统称为~。
17、单位性状:在研究性状遗传时,把植株所表现的性状总体区分为各个单位作为研究对象,这样区分开来的性状称为~。
遗传学名词解释

遗传学名词解释1、原核细胞:具有原核细胞的生物统称为原核生物2、前导链:5‘—3’方向延伸的链称为前导链。
3、冈崎片段:另一条链先沿5‘—3’方向合成的一些片段称为冈崎片段。
4、单位性状:生物所表现的性状总体区分为各个单元,这些被区分开的每一个具体性状称为单位性状。
5、复等位基因:同源染色体上相同位点上存在的3个或3个以上的等位基因称复等位基因。
6、性影响遗传:是指位于常染色体上的基因所控制的性状,是由于内分泌及其他关系使得某些性状或只出现在雌雄一方;或者一方为显性,另一方为隐形的现象。
7、遗传距离:交换值表示两个基因在同一染色体上的相对距离,叫做遗传距离。
8、嵌合体:突变体区与正常非突变性状并存在一个生物体或其器官,组织上,称为嵌合体。
9、易位:染色体上某一区域移接到其非同源染色体上10、整倍体:染色体数是x整倍数的个体或细胞称为整倍体11、初级三体:外加的染色体与其余两条染色体完全相同,即同源组的3条染色体相同。
12、QTL:控制数量性状的基因座13、加性效应:指基因位点内等位基因和非等位基因的累积效应,用A 表示14、转导:是指以噬菌体为媒介所进行的细菌遗传物质重组的过程15、部分二倍体:在接合后的一个短时间内,供体外基因子与受体内基因子形成一段二倍体的DNA,这样的细菌称为二倍体。
16、真核细胞:结构复杂,具有细胞核和细胞器的一类细胞17、相对性状这种同一单位性状在不同个体间所表现出来的相对出来的相对差异,称为相对性状。
18、后随链:冈崎片段由DNA连接酶连接起来,成为一条完整的链,这条链成为后随链。
19、遗传密码:DNA分子中含有4种密码符号,遗传信息就贮藏在4种碱基密码的不同排列顺序中,成为遗传密码。
20、芽变:植物芽原基发育早期的突变细胞可能发育形成一个突变芽或枝条,称为芽变。
21、不完全显性:有些性状,其杂种F1的性状表现是双亲性状的中间型,这称为不完全显性。
22、连锁群:存在于同一染色体上的基因群。
遗传学名词解释

遗传学: 研究生物遗传和变异现象与规律的科学遗传:指子代与亲代相似的现象。
变异:指子代与亲代之间、子代个体之间存在不同程度的差异。
同源染色体:大小及形态相同,分别来源于父本和母本的一对染色体。
非同源染色体:同一染色体群体中,形态结构不同的各对染色体之间互称为非同源染色体。
性染色体:许多物种中,还存在一对形态和结构不同的同源染色体。
常染色体:除性染色体之外的其它染色体。
每一对正常的同源染色体都具有相同的基因座。
染色体组型或核型:指由体细胞中全套染色体按形态特征(包括染色体长度、着丝点位置、臂比、随体有无等)和大小顺序(染色体长度)排列构成的图形。
有丝分裂:即体细胞分裂,通过分裂产生具有同样染色体数目的子细胞,在分裂中出现纺锤体。
减数分裂:是指在真核生物性细胞形成过程中,染色体只复制一次而细胞连续进行两次分裂使细胞的染色体数目减半的过程。
单位性状:是指将生物体所表现的总体性状区分成的每一个具体性状。
相对性状:是指同一单位性状在不同个体间所表现出来的相对差异。
显性性状:杂种F1仅表现亲本之一的性状,将F1表现出来的亲本性状;隐性性状:未表现出来的亲本性状基因型:是指个体或细胞的基因组合,是生物的内在遗传组成,如决定圆形种子性状的基因型为RR 和Rr,而决定皱形种子性状只能是rr;表现型:是指生物体所表现的性状(形态),如白花和红花性状。
等位基因:指位于一对同源染色体上,位置相同,控制同一性状的一对基因,是同源染色体同一基因座上的基因的不同形式。
复等位基因:在同源染色体的相同基因座上,存在3个或3个以上的等位基因显性基因:是指基因型处于杂合状态时,能够表现其表型效应的基因;隐性基因:是指基因型处于杂合状态时,不能表现其表型效应的基因。
纯合基因型:是指同一基因座上有两个相同的等位基因,如RR或rr;纯合体是指具有纯合基因型的个体。
杂合基因型:是指同一基因座上有两个不相同的等位基因,如Rr;杂合体是指具有杂合基因型的个体。
遗传学名词解释

1、遗传学:是研究生物遗传和变异的科学,是生物学中一门十分重要的理论科学,直接探索生命起源和进化的机理。
同时它又是一门紧密联系生产实际的基础科学,是指导植物、动物和微生物育种工作的理论基础;并与医学和人民保健等方面有着密切的关系。
2、变异:是指亲代与子代之间、子代个体之间存在着不同程度差异的现象。
如高秆植物品种可能产生矮杆植株,一卵双生的兄弟也不可能完全一样。
3、遗传:是指亲代与子代相似的现象。
如种瓜得瓜、种豆得豆。
4、冈崎片段:相对比较短的DNA链(大约1000),是在DNA的的不连续合成期间生成的片段。
5、半保留复制:一种(DNA)的复制模型,其中亲代双链分离后,每条单链均作为新链合成的模板。
6、半不连续复制:是指DNA复制时,上的合成是连续的,上是不连续的,故称为半不连续复制。
7、联会:在减数分裂过程中,同源染色体建立联系的配对过程。
8、同源染色体:指形态、结构和功能相似的一对染色体,他们一条来自父本,一条来自母本。
9、减数分裂:是生物中数目减半的分裂方式。
性细胞分裂时,染色体只复制一次,细胞连续两次,染色体数目减半的一种特殊分裂方式。
减数分裂不仅是保证染色体数目稳定的机制,同时也是物种适应环境变化不断的机制。
10、复等位基因:由同一基因位点经多方向突变产生的三个或三个以上的基因称为复等位基因。
一个基因座位内不同位点改变形成许多等位基因,即复等位基因。
复等位基因是基因内部不同碱基改变的结果。
11、复制子:在每条染色体上两个相邻复制终点之间的一段DNA叫做复制子。
12、共显性:是指双亲性状同时在F1个体上表现出来。
如人类的ABO血型和MN血型。
13、等位基因:位于同源染色体上,位点相同,控制着同一性状的基因。
14、上位作用:两对基因同时控制一个单位性状发育,其中一对基因对另一对基因的表现具有遮盖作用,这种基因互作类型称为上位作用。
15、抑制作用:指一对基因本身不表现性状,当其处于显性纯合或杂合状态时,却能够使另一对显性基因不起作用。
遗传学名词解释

名词解释1.Genetics 〔遗传学〕:研究生物体遗传与变异规律的科学。
现代遗传学是研究基因的结构、功能及其变异、传递和表达规律的科学,亦称为基因学。
2.Chromatin 〔染色质〕:是在间期细胞核内由DNA、组蛋白、非组蛋白和少量 RNA组成的 ( 线性复合结构 ) ,易被碱性染料着色的一种无定形物质 , 是间期细胞遗传物质存在的形式。
〔染色体〕:是染色质在细胞分裂过程中经过紧密缠绕、折叠、凝缩、精巧包装而形成的,具有固定形态的遗传物质的存在形式。
4.Constitutive heterochromatin〔组成性异染色质〕:通常所指的异染色质,是一种永久性的异染色质,在染色体上的位子较恒定,在间期细胞核中仍保持螺旋化状态,染色很深。
5. ※facultative heterochromatin〔兼性异染色质〕:在一定的细胞类型或一定的发育阶段呈现凝集状态的异染色质。
6.※lampbrush chromosome〔灯刷染色体〕:是未成熟的卵母细胞进行第一次减数分裂停留在双线期〔可持续数月〕的染色体。
7.※cell cycle 〔细胞周期〕:细胞分裂结束到下一次细胞分裂结束所经历的过程,这段时间称为细胞周期。
8.※Mitosis 〔有丝分裂〕:没有明显界限的细胞分裂的连续过程,可分为前期中期后期末期。
9.※Meiosis 〔减数分裂〕:性母细胞成熟时配子形成过程中发生的一种特殊有丝分裂,使体细胞染色体数目减半。
10.Character 〔性状〕:生物体的形态特征、生理生化特征的总称。
11.unit character〔单位性状〕:每一个可以具体区分的性状。
12.contrasion character〔相对性状〕:同一单位性状在不同个体间所表现出来的相对差异。
13.等位基因〔 allele 〕: 位于同源染色体上相同座位上 , 控制相对性状的一对基因。
14.基因型〔 genotype 〕 : 生物个体或细胞遗传物质的组成 , 决定生物体一系列发育性状的可能性。
遗传学名词解释

遗传学名词解释1.变异:指亲代与子代之间、子代个体之间存在的差异。
2.突变:DNA分子某些部分的基因能够发生改变,使生物产生性状的差异。
3.原核细胞:指一类结构简单、没有细胞核(仅有拟核)以及没有膜包被细胞器的细胞。
4.真核细胞:指一类结构复杂、具有细胞核和细胞器的细胞。
5.核仁:是真核细胞间期核中最明显的呈中圆形或椭圆形的颗粒状结构,其组成成分有rRNA、rDNA和核糖核蛋白。
6.染色体:指细胞分裂过程中,由染色质聚缩而呈现为一定数目和形态的复合结构。
7.染色质:指间期细胞核内由DNA、组蛋白、非组蛋白和少量RNA组成的线性复合结构,因其易被碱性染料染色而得名,是间期细胞遗传物质存在的主要形式。
8.常染色体:与性别决定无关的染色体,是成对存在的,称为常染色体。
9.性染色体:与性别决定有关的染色体。
10.常染色质:指间期细胞核内纤细处于伸展状态,并对碱性染料着色浅的染色质。
11.异染色质:指间期核内聚缩程度高,并对碱性染料着色深的染色质。
12.组成性染色质:指除复制期外均处聚缩状态的染色质。
它是由相对简单、高度重复DNA序列构成。
13.兼性染色质:指在某细胞外,或其发育的某阶段,原来的常染色质卷缩、丧失转录活性而变为异染色质。
14.着丝粒:也叫着丝点。
染色体的特定部位,细胞分裂时出现的纺锤丝所附着的位置,此部位染色较浅。
15.端粒:存在于真核细胞线状染色体末端的一小段DNA-蛋白质复合体,它与端粒结合蛋白一起构成了特殊的“帽子”结构,作用是保持染色体的完整性和控制细胞分裂周期。
16.复制原点:在基因组上复制起始的一段序列。
17.主缢痕:中期染色体上一个染色较浅而缢缩的部位,主缢痕处有着丝粒,所以亦称着丝粒区,由于这一区域染色线的螺旋化程序低,DNA含量少,所以染色很浅或不着色。
18.次缢痕:指某些染色体臂上除主缢痕外还常含有另外缢缩区域。
19.随体:是位于染色体末端的、圆形或圆柱形的染色体片段,通过次缢痕与染色体主要部分相连。
遗传学名词解释

遗传学名词解释1. 基因:生物体遗传信息的基本单位,位于染色体上。
基因决定了生物体的遗传特征。
基因:生物体遗传信息的基本单位,位于染色体上。
基因决定了生物体的遗传特征。
2. 染色体:细胞核中的细长结构,携带着遗传物质。
人类有23对染色体,其中一对性染色体决定了个体的性别。
染色体:细胞核中的细长结构,携带着遗传物质。
人类有23对染色体,其中一对性染色体决定了个体的性别。
3. 等位基因:存在于同一基因位点上的不同基因形式。
个体可以携带两个等位基因中的一种。
等位基因:存在于同一基因位点上的不同基因形式。
个体可以携带两个等位基因中的一种。
4. 显性和隐性:显性基因表现出来的特征会掩盖隐性基因的表现。
只有当个体携带两个隐性基因时,该特征才会显现出来。
显性和隐性:显性基因表现出来的特征会掩盖隐性基因的表现。
只有当个体携带两个隐性基因时,该特征才会显现出来。
5. 杂合子和纯合子:杂合子指一个位点上携带两个不同等位基因的个体,而纯合子指携带两个相同等位基因的个体。
杂合子和纯合子:杂合子指一个位点上携带两个不同等位基因的个体,而纯合子指携带两个相同等位基因的个体。
6. 基因型和表型:基因型是指个体在其基因中的特定基因组合,而表型是由基因型和环境共同决定的个体可观察到的特征。
基因型和表型:基因型是指个体在其基因中的特定基因组合,而表型是由基因型和环境共同决定的个体可观察到的特征。
7. 遗传变异:由基因突变引起的遗传信息的变化。
遗传变异是生物进化的基础。
遗传变异:由基因突变引起的遗传信息的变化。
遗传变异是生物进化的基础。
8. 杂交:不同种类或不同个体之间的繁殖,导致遗传物质的重新组合。
杂交有助于增加遗传多样性。
杂交:不同种类或不同个体之间的繁殖,导致遗传物质的重新组合。
杂交有助于增加遗传多样性。
9. 基因工程:利用分子生物学技术对基因进行改变或操控的过程。
基因工程可以创造具有特定遗传特征的生物体。
基因工程:利用分子生物学技术对基因进行改变或操控的过程。
遗传学名词解释

遗传学名词解释绪论1.变异:亲代与子代之间、子代个体之间,存在着不同程度差异的现象叫变异。
2.遗传:亲代与子代相似的现象称为遗传。
第一章1.同源染色体:形态和结构相同的一对染色体称为同源染色体。
非同源染色体:形态和结构不同的各对染色体之间,互称为非同源染色体。
2.有丝分裂:经过染色体有规律的和准确的分裂过程,分裂过程中出现纺锤丝,包括质分裂和核分裂两个过程。
3.无融合生殖:雌雄配子不发生核融合的一种无性生殖方式。
4.减数分裂:又称成熟分裂,经过两次分裂,使体细胞染色体数目减半。
5.联会复合体:是同源染色体联结在一起的一种特殊的固定结构。
6.交叉端化:交叉向二价体的两端移动,并且逐渐接近于末端的现象。
第二.三章1.单位性状:被分开的每一个具体形状称为单位性状。
2.相对性状:同一单位性状在不同个体间所表现出来的相对差异。
3.显性性状:在F1表现出来的性状叫做显性性状。
4.隐性性状:在F1未表现出来的性状叫做隐性性状。
5.不完全显性:杂种F1的性状表现是双亲性状的中间型,称为不完全显性。
6.共显性:双亲的性状同时在F1个体上表现出来,这种显性表现称为共显性。
7.自交:植物的自花授粉称为自交。
8.测交:被测验的个体与隐性纯合个体间的杂交。
9.基因型:个体的基因组合称为基因型。
10.表现型:是生物体所表现的性状,由基因型和环境共同作用。
11.基因纯合体:具有纯合基因型的个体称为基因纯合体。
12.基因杂合体:具有杂合基因型的个体称基因为杂合体。
13.分离:显性性状和隐性性状同时表现出来的现象叫做分离。
14.等位基因:位于同一同源染色体的相对位点上的两个基因称为等位基因。
15.基因互作:不同对基因间相互作用的现象称为基因互作。
16.返祖遗传:F1和F2的植株表现其野生祖先的性状的现象称为返祖遗传。
17.多因一效:许多基因影响同一个性状的表现,称为多因一效。
18.一因多效:一个基因可以影响许多性状的发育,称为一因多效。
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Explaining of genetics nouns一、Explain the following terms and concepts.1、heredity;(遗传)transmission of traits from one generation to another2、transmission genetics;(传递遗传学)is the brand dealing with the transmission of genes and genetic traits from generation to generation,and how genes recombine3、centromeres; (着丝点)each chromosome often has a constriction along its length4、zygote;(合子)the cell produced by the fusion of male are female gametes5、autosomes; (常染色体)chromosomes other than sex chromosome6、sister chromatid; (姐妹染色单体)a chromatud denved from replication of one chromosome during interphase of the cell cycle7、chromatin; (染色质)the mixture of DNA and protein8、semiconservative replication;(半保留复制)a model of DNA replication in which a double-stranded molecule replocates in such a way that the daughter moleculars are composed of one parental(dd)and one nemly synthesized serand9、the replication fork; (复制叉)the region where the helix unwinds and new DNA10、replicon; (复制子)DNA replicated from a single origin11、codon; (密码子)the DNA sequence of a gene is divided into a series of units of three bases12、degeneracy; (简并)the number of codons is greater,all of the amino acids,with the exception of methionine and typtophan,are encodoned by more that one codon13、hereditary traits; (遗传性状)the characteristics of an individual that one transmitted from one generation to another14、Genotype; (基因型)the genetic constitution of an organism15、phenotype; (表现型)is the observable properties(structural and functional)of organism produced by the interaction between its genotype and the environment16、pure-breeding lines; (纯种品系)this refers to organisms which have been inbred for many generations in which a certain phenotype remains the same17、dominance;(显性)in hybrids between two individuals with different phenotypes only ine phenotype may be observed18、testcross; (测交)is a cross of an individual of unknown genetype (usually expressing the dominant phenotype)with a known homozygous recessive individual in order to determine the unknown genetype19、the dihybrid cross;(双因子杂交)a cross involving two pairs of contrasting traits20、complete dominance; (完全显性)is the phenoment in which one alleles is dominant to another,so that the neterozygote(F1)is the same as that of the homozygous dominant 21、incomplete dominance; (不完全显性)expression of heterozygous(F1)phenotype which is distinct from and often intermediate to that of either parent22、multiple alleles; (复等位基因)three or more alleles of the same gene23、epistasis; (上位作用)is a from of gene interaction in which one gene masks the phenotypic expression of another24、linkage; (连锁)is the tendency of for alleles of two or more genes to be passed together from one generation to the next25、recombination frequency;(重组率)is the ratio of recombinant gametes to all the gametes produced in meiosis26、coupling phase; (相引组)the two dominant alleles are on one homolog and the two recessive alleles are on the other homolog,an arrangement27、repulsion phase; (相斥组)each homolog carries the dominant allele of one gene and the recessive allele of the other gene,an arrangement28、incomplete linkage; (不完全连锁)o ccasional separation of two genes on the same chromosome by a recombinational event29、crossing over; (交换)thw exchange of chromosomal material (parts of chromosomal arms)between homologous chromosomes by breakage and reunion30、genetic map; (遗传图)a replesentation of the genetic distance separating nonalleic gene loci in a linkage structure31、two-point testcross; (两点测验)a test involving two gened within a relatinely short section of the chromosome32、three-point testcross; (三点测验)a test involving three genes within a relatively short section of the chromosome33、sex chromosome; (性染色体)is a chromosome such as X or Y in hurnans ,which is involved in sex determinate34、sex-limited triaits(限性性状)in some cases,the expression of a specific phenotype is absolutely limited to one sexsex-influenced traits;(性别影响性状)means that the same phenotype will occur in both sexes but is more common in one35、spontaneous mutations (自发突变)are these that just happen in natureinduced mutations; (诱发突变)that reault from the influence of any artificial factor36、gametic mutations (配子诱变)a mutation event occurring in gametes or gamete-forming tissuessomatic mutations; (细胞诱变)a mutation event occurring in a somatic cell37、forward mutations (正突变)a mutationed change from a wild-type allele to a mutation allele, in general,A-areverse mutations; (反突变)a mutation change from a mutant allele back to a wild-type allele, in general, a-A38、point mutation; (真突变)a mutation that can be mopped to a single locus ,at the molecular level,a mutation that results in the substitution of one nucleotide for another 39、transition; (转换)a mutation event in which one purine is replaced by anpther or are pyrimidine is replaced by another40、transversion; (颠换)a mutational event in which a purine is replaced by a pyrimidine or a primidine is replaced by a purine41、missense mutations; (错义突变)these point mutations involve the alteration of a single base which changes a codon such that the encoded amino acid id altered42、nonsense mutations; (无义突变)these are point mutations that charge a codon for an amino acid a termination codon43、silent mutations ;(沉默突变)mutations many occour at the third base of a codon and ,due to the degeneracy of the genetic code,the amino acid will not be altered44、frameshift mutations; (移码突变)is a mutational event leading to the insertion ordeletion of one or more bases in a gene,shifting the codon reading frame in all codons following the mutational site45、transposable element; (转座因子)a genetic element of chromosomes of both prokaryotes and eukaryotes that has the capacity to mobilize itself and move from one location to another in the genome46、deletion;(缺失)a deletion is a chromosome mutation in which part of a chromosome is missing47、duplication; (重复)A chromosomed aberration in which a segment of the chromosomeB repeated48、inversion; (倒位)is a type of chromosomal aberration in which a segment of a chromosome is turn around 180 within a chromosome49、Robertsonian fusion;(罗伯孙融合)two telecentric chromosome or acro centric chromosomes, may fuse at the centromeres to give one metacentric or submetacentrec chromosome,reducing the number of chromosomes50、karyotypes; (核型)a complete set of all the metaphase chromosomes ina cell51、nullisomy; (缺体)describes an individual with a chromosomal aberration in which both members of a chromosome are missing.the cell is 2n-252、monosomy; (单体)an aneuploid conditive in which one member of a chromosome pair is missing 2n-153、trisomy; (三体)an aneuploid condition in which there are three copies of a particular chromosome instead of two copies 2n+154、tetrasomy; (四体)invlives an extra chromosome pair ,resulting in the presence of four copies of one particular chromosome and two copies of other chromosomes2n+255、autopolyploidy (同源多倍体)polyploidy involving more than two chromosomes sets of the same speciesallopolyploidy; (异源多倍体)polyploidy involving two or more genetically distinct sets of chromosomes56、qualitative trait (质量性状)traits such as these,withonly a few distinct phenotypes,area called discontinuous traits ,or qualitative traitsquantitative trait; (数量性状)traits with a continuous distribution of phenotypes are called continuous traits or quantitative traits57、Heterosis;(杂种优势)the superiority of a hererozygote over either homozygote for one or more characters58、virulent phages (烈性噬菌体)phages that undergo lytie infection are called virulent phagestemperate phages; (温和噬菌体)phages that undergo lysogenic infection are said to be temperate59、tansformation; (转化)it is possible to transfer DNA extracted from one bacterial culture to recipient in vitro .This is a process as transformation60、conjugation; (接合)a process in which there is a unidirectional transfer of genetic information through direct celluar contract between a clonor bacterice cell and a recipient bacterial cell61、F+ factor:the bacteria that contain the F plasmidF- factor:that bacteria that lack the plasmidHfr bacteria,:bacteria with integrated F plasmid are referced to HfrF' factor:the F plasmid is sometimes known as the F' factor62、transduction; (转导)under certain conditions bacteria phages can facilitate the transfer of genes between bacteria,the process is known as transduction63、operon; (操纵子)a genetic unit that consists of one or more structural genes whose expressions are negulated together by operator-regulator peotein interactives, plus the operator region itself and the promoter64、cytoplasmic inheritance;(胞质遗传)transmission of traits by genetic information contained in cytoplasmic organelles such as mitochondria and chloroplasts is known as this65、cytoplasmic-nuclear male sterility (雄性质核不育性)is controlled by both cytoplasmic genes and nuclear genesnuclear male sterility; (雄性核不育性)is mostly controlled by a single nuclear recessive gene ,but it may also be controlled by several genes,can be restored by the dominant gene contasting66、maternal effects; (母性影响)the phenotype in an indicidual that is established by the maternal nuclear genome,as the result of mRNA and /or proteins that are deposited in the occyty prior to fertilization67、population; (群体)is a groupo of individuals from the same species that lives in the same geographic area, and that actually or potentially interbreeds68、allele frequencies (等位基因频率)the frequency of an allele(A) in a population is the number of A alleles divided by the total number of alleles of that gene locusgenotype frequencies; (基因型频率)we count the number of individuals with one particular genotype and divided this number by the total number of individuals in the population 69、migration (迁移)migration occurs when individuals more between the populations genetic drift; (遗传漂变)random variation in allele frequency from generation to generation70、genetic species, (遗传学种)the genetic definition of a species is a set of actudlly or potentially interbreeding organisms,and sharing a common gene poolmorphological species (形态学种)all members of a species share a set of physicalcharacteristics which can distinguish them from members of other species ecological species (生态学种)each species uses a particular set of resources ,a niche,from that environment,and they do this most efficiently in a particular set of conditions or habitat71、Genome (染色体组)the complement of genetic information in a chromosome set.72、homologous chromosomes (同源染色体)in diploid organisms,the members of a chromosome pair that contain the same genes and that pair at meiosis are called homologous chromosomes73、bivalents (二价体)the bivalents lie across the equator of the cell74、complementary base pairing (碱基互补配对)two bonds from between A and T and three between G and C ,thus G-C bonds are stronger than A-T bonds,The way in which thebases from pairs between the two DNA strands is known as it75、Intergenic DNA: (基因间DNA)the genes are very dispersed and are separated from each other by sequences that do not appear to contain useful information76、template strand (模板链)only one of the two strands of the DNA double helix carriesan RNA molecule of a polypeptide77、Introns(内含子)one of the more surprising features of genes is that in higher organisma the coding information are separated by sequences that do not contain useful informationexons (外显子)one of the more surprising features of genes is that in higher organisms the coding information is usually split into a series of segments of DNA sequence78、Nucleosomes (核小体)are the basic building blocks of chromstin structure cinsisr ofa core of histone around which DNA is79、Euchromatin. (常染色体)it is a chromatin that stains lightly.It is uncoiled during interphase but becomes condensed during mitosis80、Heterochromatin (异染色体)It is chromatin that stains darkly is genetically inactive,either because it contains no genes or because the genes it does contain cannot be expressed81、constitutive heterochromatin (组成型异染色体)same chromatin is hetero chromatic in all tissues and all stages of developmentfacultative heterochromatin (兼性异染色体)some regions of chromatin exist in either the heterochromatic or euchromatic state82、synonymous codons. (同义密码子)codons which specify the same amino acid83、The central dogma (中心法则)the biological information in a DNA molecule is contained in its base sequence and states that the infoemation is transferred from DNA to RNA to protein84、Complete dominance(完全显性)is the phenotype in which one alleles is domoninant to another ,so that theheterozygote(F1)is the same as that of the homozygous dominant85、co-dominance (共显性)the heterozygote(F1)exhibits the phenotypes of both homozygotes(parents)86、lethal allele (致死等位基因)an allele that results in the death of an organism87、the coefficient of coincidence(并发系统)the observed frequency of double cross-overs divided by the expected frequency of double cross-overs. S=0.58[0,1]88、Hemogametic (同型配子的)means that with respect to sex chromosomes gametes are all identical89、gene mutations . (基因突变)mutations in the sequences of genes at the level of the base pair90、Mutation rate (突变率)is the number of occurrence of a kind of 、mutation expressed as the proportion of cells or individuals in a population91、Wild-type (野生型)an organism that displays the usual phenotypr for that species92、Mutant (突变型)an organism whose usual phenotype has changed as the result of a mutation93、Mutagen (诱变剂)any physical or chemical agent that significantly increases the frequency of mutational events a spontaneous mutation rate94、Insertion sequences (插入序列)is the simplest transposable element found in prokaryetes. These DNA segments are relatively short, not exceeding 2000bp.The first insertion sequence to be characterized in E.coil,IS1,is 768bp long ,IS2,3,4and 5 are about 1250~1400bp long95、composite transposons (复合型转座子)have a central region containing genes flanked on both sides by IS elementsnoncomposite transposons (非复合型转座子)exemplified by the 4957bpTn3,also contain genes such as those for drug resistance they do not terminate with IS elements96、Terminal deletions (顶端缺失)invdue a single break,then the fragment with a centromere obtaining a new telomere97、Interstitial deletions (中间缺失)involve by rejoining of the ends of the flanking pieces98、paracentric inversion (臂内倒位)if the centromere isnot part of the inverted segment pericentric inversion (臂间倒位)if the centromere is part of the inverted segment99、inversion heterozygotes (倒位杂合体)organisims with one inverted chromosome and one noninverted homdog100、Translocation (易位)the movement of a chromosomal segment to a new location in the genome101、Simple translocation (简单易位)a chromosomal aberration in which a segment within a chromosome move into an nontromologous chromosome102、Reciprocal translocation (相互易位)a chromosomal aberration in which a nonhomologous chromosomes exchange parts103、Robertsonian fusion(Robertsonian融合)Fusion of two acrocentric chromosomes at the centromere.104、euploid (整倍体)when an organism or cell has one complete set of chromosomes or an exact multiple of complete sets ,that organism or cell105、aneuploid (非整倍体)chromosome mutations resulting in variations in the number of individual chromosomes produce106、Polyploidy(多倍性)is the state of having more than two complete sets of chromosomes107、Autoallopolyploids(同源异源多倍体)indicate that a polyploidy individual has more than two basic genomes ,and at least one basic genome is present more than two times108、H eritability : (遗传力)the proportion of phenotypic variation in a population attributable to genetic factors109、Broad sense heritability (广义遗传力)is the ratio of the genetic variance to the total phenotypic variance,therefore110、Narrow sense heritability (狭义遗传力)the proportion of the phenotypic variance that results from additive genetic variance111、Inbreeding(近交)is mating between relatives,or in extreme cases,self-fertilization by hermaphrodites112、episomes(附加体)we refer to plasmids that can exist in these two states113、sexduction . (性导)F primes are capable of moving to F-bacteria and in so doing bring their complement of host genes with them114、cotransduction (共转导)two genes that are close enough on the bacterial chromosome can be simultaneously transduced,a process called contransduction115、Specialized transduction (特殊性转导)genetic transfer of only specific host genes by transducing phages116、gene pool(基因库)is the total of all alleles possessed by reproductive members of a population117、the Hardy-weinberg law (哈迪温伯特规律)the principle that both gene and genotype frequencies will remain in equilibrium in an infinitely large population in the absence of mutation,migration,selection,and nonrandom mating118、Natural selection (自然选择)is the constraint that natural conditions put on the size of populations,forcing individuals of the same species to compete for limited119、Stabilizing selection .(稳定化选择)tends to favor intermediate types,with both extreme phenotypes being selection against120、Directional selection (定向选择)favors individuals with characteristics at one end of the range found in the population121、Disruptive selection (分裂选择)is selection against intermediates and for both phenotypic extreams.It can be viewed as the opposite of stadilizing selection because the intermediate types are selected against122、Random mating (随机交配)all the gametes unite to form zygotes,the proportion of the genotypes will be equal to p2,2pq and q2 ,and the frequency of the alleles un these zygotes will remain p and q123、Premating isolation mechanisms(交配前隔离机制)prevebt interbreeding and zygote formation124、Postmating isolation mechanisms (交配后隔离机制)reduce the viability and/or fertility of hybrids produced by mating between members of two species125、H ybrid inviability (杂种不存活)hybrids zygote are inviable or have reduced viability 126、Hybrid sterility (杂种不育性)one or both sexes of the F1 hybrids are sterile or have reduced fertility127、H ybrid breakdown (杂种败落)F1 hybrids are normal,vigorous,and fertile but F2 or backcross hybrids are inviable,sterile,or have reduced viability or fertility128、Speciation (物种形成)is the process of forming two or more species from a single 129、Allopatric speciation (异地种形成)process of speciation associated with geographic isolation130、Sympatric speciation (同地种形成)process of secration involving population that inhabit,at least in part,the same geographic range131、N egative control: (负调控)if there exists the repressor represses the transcription of the structural genes,this mechanism is known as negative control132、Positive control(正调控)a regulation mechanism in which the transcription of the structural genes is incluced by an inducer133、trans-acting factors (反式作用因子)the transcription factors are synthesized in the cytoplasm of the cell but exert their effects in the nucleus134、Plasmon(细胞质基因组)all the genetic materials present in organelles and cytoplasmic particles are known as these135、Population genetics(群体遗传学)population genetics is the quantitative study of the frequencies of alleles and genotypesin populations,wheras evolution is the change in thoes frequencies over time。