武汉大学分子生物学_2004期末试卷A

武汉大学分子生物学_2004期末试卷A
武汉大学分子生物学_2004期末试卷A

武汉大学生命科学学院

2003-2004学年第一学期期末考试

《分子生物学》试卷

Final exam of Molecular Biology Course (Spring 2004)

年级______ 专业________ 学号_________ 姓名_______成绩______ PART I: DESCRIPTION (2 points each)

Your answer should describe what each item is and how it functions in the cell. Diagrams, structure and sequence information should be included in your answer, as necessary.

1.Yeast artificial chromosome

2.RNA interference

3.Proteomics

4.Shine-Dalgarno sequence

5.Alternative splicing

6.Ribozyme

7. -dependent termination

8.RNA editing

9.DNA lesions

10.Protein targeting

PART II: MULTIPLE CHOICES (1 points each)

Select the one best answer for each question.

1. The catalytic activity for peptide bond formation (the peptidyl transferase activity) is

located in the:

1)RNA of the large ribosomal subunit.

2)leader sequence of the messenger RNA.

3)RNA of the small ribosomal subunit.

4)proteins of the small ribosomal subunit.

5)proteins of the large ribosomal subunit.

2. Bidirectional and semi-conservative are two terms that refer to:

1)transcription.

2)translation.

3)replication.

4)all of the above.

5)none of the above.

3. The fact that most amino acids are specified by multiple codons is known as:

1)the “wobble” phenomenon.

2)the universality of the genetic code.

3)codon bias.

4)the anticodon hypothesis.

5)the redundancy of the genetic code.

4. RNA polymerase I is the eukaryotic enzyme responsible for:

1)transcription of ribosomal RNA.

2)transcription of transfer RNA and other small RNA species.

3)transcription of messenger RNA.

4)initiation of Okazaki fragment synthesis in DNA replication.

5. Restriction enzymes can cleave DNA that is either single-stranded or double-stranded,

as long as it contains the appropriate recognition site.

1) True 2) False

6. Information about the sequence of the coding region of a gene is best obtained from:

1) a YAC clone.

2) a genomic clone.

3) a cDNA clone.

4)the protein.

7. A chromatography method that can be used specifically to purify proteins based on their

charge is:

1)gel filtration chromatography.

2)ion-exchange chromatography.

3)DNA affinity chromatography.

4)antibody affinity chromatography.

8. A nonsense mutation is a change in the DNA sequence that results in:

1) a small deletion or insertion.

2)an amino acid change in the protein encoded by the gene.

3) a premature stop codon.

4)all of the above.

5)none of the above.

9. A protein complex involved in degradation of proteins within the cell is known as the:

1)ubiquitin/proteasome system.

2)molecular chaperone.

3)chaperonin.

4)ribosome.

5)Krebs/TCA cycle.

10. ___binds to the repressor and turn on the transcription of the structural genes in the

Lac operon.

1)cAMP

2)lactose

3)allolactose

4)CRP

11. Which of the following RNA species is involved in degradation of the mRNA

containing complementary sequence

1)miRNA

2)siRNA

3)tRNA

4)5S RNA

5)U3 snRNA

12. The genome sequencing projects are confirming the theory that genome size is directly

proportional to the number of genes contained within that genome. In other words, a genome that is 10 times as big will contains approximately 10 times as many protein coding genes.

1) True 2) False

13. HeLa cells, derived from a human cervical carcinoma, are able to propagate

indefinitely in culture and are therefore known as a(n):

1)tissue culture.

2)tumor.

3)transgenic cell line.

4)immortalized cell line.

14. E. coli cells are smaller than yeast cells.

1) True 2) False

15. Which of the following domains is not a DNA binding domain

1)Proline-rich domains

2)Helix-turn helix domains

3)Zinc finger domains

4)Basic domains

16. The aminoacyl-tRNA synthetases distinguish between about 40 different shaped tRNA molecules in the cells.

1) True 2) False

PART III: SHORT QUESTIONS (8 points each)

1.How do bacterial replication start and accomplished. Remember to include the

proteins/enzymes and important DNA sequence involved in this process.

2.Design experiments to clone a yeast gene and express this gene in yeast.

3.Below is the multiple cloning site (MCS) of the plasmid vector pUC18 and the

N-terminal and C-terminal sequence of protein X. Note that the MCS constitutes a part of the LacZ open reading frame. Suppose that you are going to clone the protein X gene into pUC18, so that your target gene is transcribed under the control of LacZ

promoter, and translated with the LacZ gene to produce a fusion protein. You are

requested to use Bam HI and Pst I to the clone X gene, please add these restriction sites on the corresponding position of the X gene. Remember to maintain the

reading frame of the X gene with the LacZ gene

4.

(1) MCS of pUC18

Eco RI Sac I Kpn I Sma I Bam HI Xba I Sal I Pst I

ACG AAT TCG AGC TCG GTA CCC GGG GAT CCT CTA GAG TCG ACC TGC AGG CAT GCA

Thr Asn Ser Ser Ser Val Pro Gly Asp Pro Leu Glu Ser Thr Cys Arg His Ala

Lac Z

(2) N-terminal sequence of X gene. ATG ACC CCU CAU AAC GGC GAC…

Met Thr Pro His Asn Gly Asp…

(3) C-terminal sequence of X gene. …GAU AGU ACA GCU GCC AAG TAA

…Asp Ser Thr Ala Ala Lys

PART IV: MAJOR QUESTIONS (20 points each)

1: Please describe how an mRNA gene is transcribed, processed and translated in human cells. What are the possible mechanisms in regulating the expression of this gene?

2 (20 points): A bacterium is found to metabolize a rare sugar produced by a plant that the bacteria grow on. However, the bacteria prefer glucose as the energy source. The problem is, if you want to finish this course with a satisfied score, you must figure out the regulatory mechanism that the bacteria used to determine the sugar choice.

The gene involving in the rare sugar metabolism has been identified as fun3. You can use northern blot to analyze the expression of fun3 and use DNA footprinting to analyze the binding of proteins to the control elements of fun3 gene. The following table shows the experimental results

Questions:

1.Please propose a mechanism to explain the above results. You should focus on the

question “How does the expression of fun3 gene is tightly regulated so that it is only highly expressed when the rare sugar is the only carbon source”. You must answer what proteins A, B and C are. (8 points)

2.How is protein A regulated? (2 points)

(1)glucose turns the repressor on

(2)glucose turns the repressor off

(3)the rare sugar turns the repressor on

(4)the rare sugar turns the repressor off

3.How is protein C regulated? (2 points)

(1)glucose turns the activator on

(2)glucose turns the activator off

(3)the rare sugar turns the activator on

(4)the rare sugar turns the activator off

4. How could you make the bacteria always use the rare sugar as the energy source even in the presence of glucose? (8 points)

武汉大学生命科学学院

2003-2004学年第一学期期末考试

《分子生物学》试卷及参考答案

Final exam of Molecular Biology Course (Spring 2004)

写在参考答案前面的话:

该课程考试目的是考查学生对所学知识掌握的情况,除选择题外,其他题目的答案基本都不是唯一的。你可以从不同的角度去阐明一个概念。

公布参考答案的目的:为该课程画个句号,让学生过个安心暑假

Best wishes to all of you

PART I: DESCRIPTION (2 points each)

Your answer should describe what each item is and how it functions in the cell. Diagrams, structure and sequence information should be included in your answer, as necessary.

1.Yeast artificial chromosome:

①酵母人工染色体(0.5 point)

②contains components required for replication and segregation of the natural yeast

chromosome, including two telomeric sequences (TEL), one centromere (CEN)

and one autonomously replicating sequences (ARS) (0.75 point )

③contains genes act as selective markers in yeast and proper restriction sites (0.75

point )

④can accommodate genomic DNA fragments of more than 1 Mb (0.5 point)

2.RNA interference:

①RNA干扰(0.5 point)

② a conserved biological response to double-stranded RNA (1 point)

③regulates the expression of protein-coding genes through siRNA or miRNA (1

point)

④the dsRNA is restricted by DICER, then RISC mediates the siRNA and miRNA

related RNA degradation and translation inhibition, respectively. (1 point)

3.Proteomics

①蛋白组学(0.5 point)The study of the proteome using techniques of high

resolution protein separation and identification (1.5 point)

④The best separation method is two dimensional gel electrophoresis, the individual

protein spots are then cut from the gel and treated with protease to produce a set of peptides characteristic of that protein. The precise masses of each peptide in the

sample are then determined by MALDI mass spectrometry. The resulted peptide

mass fingerprint of that protein is then compared to a database to deduce the

function of that protein etc. (1.5 point)

4.Shine-Dalgarno sequence

①SD 序列(0.5 point)

② A conserved sequence 8-13 nt upstream of the first codon to be translated (1

point).

③This sequence was discovered by Shine and Dalgarno (0.5 point)

④The sequence is purine-rich and contains all or part of 5’-AGGAGGU-3’ (0.5

point)

⑤Can base-p air with the 3’-end of the 16S rRNA (0.5 point)

5.Alternative splicing

①可变剪接(0.5 point)

②The generation of different mature mRNAs from a particular type of gene

transcript by choosing different 5’- and 3’-splice sites (2 point).

6.Ribozyme

①核酶(0.5 point)

②an RNA molecule capable of catalyzing a chemical reaction (2 point).

7.ρ-dependent termination

①ρ-依赖型转录终止(0.5 point)

②During bacterial transcription, some terminator sites do not form strong hairpins,

thus termination of the transcription by bacterial RNA polymerase requires

the assistance of an accessory factor called rho (ρ) protein (2 point).

8.RNA editing

①RNA编辑(0.5 point)

② A form of RNA processing in which nucleotide sequence of the primary

transcript is altered by either changing, inserting or deleting residues at the

specific points along the molecule (2 point).

9.DNA lesions

①DNA损伤(0.5 point)

②An alteration to the normal chemical or physical structure of the DNA (2 point).

③The lesions can lead to cell death or DNA mutation (1 point).

10.Protein targeting

①蛋白定位(0.5 point)

②Synthesis of eukaryotic proteins is usually occurred in cytoplasm (0.5 point).

③However, many proteins need to be transported to specific cellular locations, such

as nucleus, mitochondrion or chloroplast, to exert their biological functions. This

process is called protein targeting (1 point).

④The ultimate cellular location of proteins is often determined by specific, relative

short, amino acid sequences within the proteins themselves. The sequence inside

of a protein determining the cellular location of the protein is called signal

sequence (1 point).

PART II: MULTIPLE CHOICES (1 points each)

Select the one best answer for each question.

1. The catalytic activity for peptide bond formation (the peptidyl transferase activity) is

located in the:

1)RNA of the large ribosomal subunit.

2)leader sequence of the messenger RNA.

3)RNA of the small ribosomal subunit.

4)proteins of the small ribosomal subunit.

5)proteins of the large ribosomal subunit.

2. Bidirectional and semi-conservative are two terms that refer to:

1)transcription.

2)translation.

3)replication.

4)all of the above.

5)none of the above.

3. The fact that most amino acids are specified by multiple codons is known as:

1)the “wobble” phenomenon.

2)the universality of the genetic code.

3)codon bias.

4)the anticodon hypothesis.

5)the redundancy of the genetic code.

4. RNA polymerase I is the eukaryotic enzyme responsible for:

1)transcription of ribosomal RNA.

2)transcription of transfer RNA and other small RNA species.

3)transcription of messenger RNA.

4)initiation of Okazaki fragment synthesis in DNA replication.

5. Restriction enzymes can cleave DNA that is either single-stranded or double-stranded,

as long as it contains the appropriate recognition site.

1) True 2) False

6. Information about the sequence of the coding region of a gene is best obtained from:

1) a YAC clone.

2) a genomic clone.

3) a cDNA clone.

4)the protein.

7. A chromatography method that can be used specifically to purify proteins based on their

charge is:

1)gel filtration chromatography.

2)ion-exchange chromatography.

3)DNA affinity chromatography.

4)antibody affinity chromatography.

8. A nonsense mutation is a change in the DNA sequence that results in:

1) a small deletion or insertion.

2)an amino acid change in the protein encoded by the gene.

3) a premature stop codon.

4)all of the above.

5)none of the above.

9. A protein complex involved in degradation of proteins within the cell is known as the:

1)ubiquitin/proteasome system.

2)molecular chaperone.

3)chaperonin.

4)ribosome.

5)Krebs/TCA cycle.

10. ___binds to the repressor and turn on the transcription of the structural genes in the

Lac operon.

1)cAMP

2)lactose

3)allolactose

4)CRP

11. Which of the following RNA species is involved in degradation of the mRNA

containing complementary sequence

1)miRNA

2)siRNA

3)tRNA

4)5S RNA

5)U3 snRNA

12. The genome sequencing projects are confirming the theory that genome size is directly

proportional to the number of genes contained within that genome. In other words, a genome that is 10 times as big will contains approximately 10 times as many protein coding genes.

1) True 2) False

13. HeLa cells, derived from a human cervical carcinoma, are able to propagate

indefinitely in culture and are therefore known as a(n):

1)tissue culture.

2)tumor.

3)transgenic cell line.

4)immortalized cell line.

14. E. coli cells are smaller than yeast cells.

1) True2) False

15. Which of the following domains is not a DNA binding domain

1)Proline-rich domains

2)Helix-turn helix domains

3)Zinc finger domains

4)Basic domains

16. The aminoacyl-tRNA synthetases distinguish between about 40 different shaped tRNA molecules in the cells.

1) True 2) False

PART III: SHORT QUESTIONS (8 points each)

1.How do bacterial replication start and accomplished. Remember to include the

proteins/enzymes and important DNA sequence involved in this process.

Initiation (3 points):

a)replication of the bacterial chromosome is tightly coupled to the growth cycle.

b)The E. coli origin is within the genetic locus oriC that contains four 9 bp binding

sites for the initiator protein DnaA.

c)Synthesis of DnaA is coupled to growth rate so that the replication of the bacterial

chromosome is coupled to the growth cycle.

d)Once the cellular level of DnaA reaches a critical level, DnaA protein forms a

complex of 30-40 molecules at the oriC DNA, which facilitates melting of three

13 bp AT-rich repeat sequences to allow binding of DnaB protein.

e)DnaB protein is a DNA helicase that utilizes the energy of ATP hydrolysis to

melt dsDNA.

f)The ssDNA created by DnaB is coated with single-stranded binding protein (Ssb)

to protect it from breakage and to prevent the DNA renaturing.

g)The DNA primase then attaches to the DNA and synthesizes a short RNA

primer to initiate synthesis of the leading strand of the first replication fork.

Unwinding (1 point)

i.For replication to proceed away from the origin, DNA helicases must travel

along the template strands to open the double helix for copying, which is

accomplished by the joint efforts of DnaB and Ssb.

ii.Unwinding causes positive supercoiling of the unwound DNA; the positive supercoiling is relaxed continuously by the introduction of further negative

supercoils by type II topoisomerase called DNA gyrase.

Elongation (3 points)

a)Initiation of the replication of the lagging strand. As the newly formed replication

fork displaces the parental lagging strand, a mobile complex called a primosome, which includes the DnaB helicase and DNA primase, synthesizes RNA primers

every 1000-2000 nt on the lagging strand.

b)Both leading and lagging strand primers are elongated by DNA polymerase

III holoenzyme. This multisubunit complex is a dimmer, one half synthesizing

the leading strand and the other the lagging strand.

c)Lagging strand synthesis. DNA polymerase III holoenzyme:α subunit -the actual

polymerase, ε-a 3’→5’ proofreading exonuclease. DNA polymerase I removes the lagging strand primers and fills in the resulted gaps. DNA ligase makes the final

phosphodiester bond between fragments.

Termination and segregation (1 points)

i.Two replication forks meet at the terminator sites (terminus)

ii.tus gene product binds to the terminus and acts as an inhibitor of DnaB helicase.

iii.When replication is completed, the two interlinked daughter circles are unlinked by topoisomerase IV.

2.Design experiments to clone a yeast gene and express this gene in yeast.

Clone (4 points):

a)PCR amplification of the gene of interest, including two proper restriction sites at

the ends of the PCR amplified DNA

b)Choose a cloning vector: it could be a regular cloning vector that is capable of

propagating in E. coli, easy to extract from E. coli and manipulated in test tubes.

It could also be a shuttle and expression vector that also contains the yeast 2μ

origin to allow the plasmid replication in yeast, the selective marker to allow the

plasmid containing cells grow, the promoter to allow the gene of interest to be

transcribed, a poly(A) site for addition of poly(A) tail on the transcript.

No matter what type of the vector is chosen, plasmid shall be prepared from the E.

coli cells.

c)Restriction digestion of both plasmid and the gene of interest with the same

restriction sites.

d)Ligation and transformation

e)Selection and identification of the transformants to obtain the clone containing the

right recombinant plasmid.

Expression (4 points):

f)If a shuttle and expression vector is chosen as described in step②, the expression

process will include 1preparation of the recombinant DNA from E. coli cells,

2transformation of yeast cells with the recombinant DNA, 3selection of the

transformants, 4growth of the transformants, 5expression of the gene by induction

of the transcription from the promoter and 6detection of the expressed RNA and/or protein. Induction is not required if a constitutive promoter is used. (4 points)

g)If a regular cloning vector is chosen as described in step②, a subclone need to be

obtained to allow the gene of interest being cloned into a shuttle and expression

vector same as described in step②. Then expression is performed the same as

described in ⑥.

3.Below is the multiple cloning site (MCS) of the plasmid vector pUC18 and the

N-terminal and C-terminal sequence of protein X. Note that the MCS constitutes a part of the LacZ open reading frame. Suppose that you are going to clone the protein X gene into pUC18, so that your target gene is transcribed under the control of LacZ

promoter, and translated with the LacZ gene to produce a fusion protein. You are

requested to use Bam HI and Pst I to the clone X gene, please add these restriction sites on the corresponding position of the X gene. Remember to maintain the

reading frame of the X gene with the LacZ gene

(1) MCS of pUC18

Eco RI Sac I Kpn I Sma I Bam HI Xba I Sal I Pst I

ACG AAT TCG AGC TCG GTA CCC GGG GAT CCT CTA GAG TCG ACC TGC AGG CAT GCA

Thr Asn Ser Ser Ser Val Pro Gly Asp Pro Leu Glu Ser Thr Cys Arg His Ala

Lac Z

(2) N-terminal sequence of X gene. ATG ACC CCU CAU AAC GGC GAC…

Met Thr Pro His Asn Gly Asp…

(3) C-terminal sequence of X gene. …GAU AGU ACA GCU GCC AAG TAA

… Asp Ser Thr Ala Ala Lys

ANSWER: G GAT CC N ATG ACC CCU CAU AAC GGC GAC (N-terminus)

GAU AGU ACA GCU GCC AAG TAA C TGC AG (C-terminus)

PART IV: MAJOR QUESTIONS (20 points each)

1: Please describe how an mRNA gene is transcribed, processed and translated in human cells. What are the possible mechanisms in regulating the expression of this gene?

a)Transcription: focusing on transcription initiation described on p222 of the

text book. (5 points)

b)Processing:5’ cappin g (addition of a m7G to the 5’ end of the RNA pol II

transcript catalyzed by mRNA guanyltransferase/capping enzyme ) (1.5 point),

intron splicing (removal of intron by splicesome that contains 5 snRNAs and

many proteins. First step- cleavage at 5’ splice site and the conserved A being

linke d to the 5’-end of the intron, second step-3’cleavage and exon ligation)

(2 points), 3’cleavage and polyadenylation (First-assembly of the

recognition complex on the polyadenylation site, second-poly(A)

polymerase/PAP cleaves the transcript at this site, third- PAP adds up to 250

A residues to the 3’end of the transcript) (1.5 point).

c)Translation: Initiation, elongation and termination (p276, 278) (5 points)

d)Regulation: Firstly, regulation can occur at the transcription level, for

example, through interaction of the transcription factors with the promoter or

URE to activate or repress the transcription (2.5 point). Secondly, regulation

can occur at the post-transcription level, for example, alternative transcription

or alternative poly(A) site (2.5 points).

2 (20 points): A bacterium is found to metabolize a rare sugar produced by a plant that the bacteria grow on. However, the bacteria prefer glucose as the energy source. The problem is, if you want to finish this course with a satisfied score, you must figure out the regulatory mechanism that the bacteria used to determine the sugar choice.

The gene involving in the rare sugar metabolism has been identified as fun3. You can use northern blot to analyze the expression of fun3 and use DNA footprinting to analyze the binding of proteins to the control elements of fun3 gene. The following table shows the experimental results

Questions:

1.Please propose a mechanism to explain the above results. You should focus on the

question “How does the expression of fun3 gene is tightly regulated so that it is only highly expressed when the rare sugar is the only carbon source”. You must answer what proteins A, B and C are. (8 points)

Pr otein A-repressor, protein B-RNA polymerase, protein C-CRP/CAP

Regulatory mechanism:

i.In the absence of rare sugar, the repressor protein binds to the promoter

region preventing the binding of RNA polymerase, transcription of the

fun3 gene is not possible. Therefore, no fun3 RNA is observed.

ii.In the presence of rare sugar, repressor protein cannot bind to the promter, allowing the RNA polymerase to bind and initiate transcription. However,

the promoter of the fun3 gene may be a weak promoter, transcription is

not efficient in the absence of activator. The activator of the fun3 gene

transcription is regulated by glucose level. The absence of glucose

activates the activator protein and allows the protein binding upstream of

the promoter to activate the transcription of fun3.

2.How is protein A regulated? (2 points)

(1)glucose turns the repressor on

(2)glucose turns the repressor off

(3)the rare sugar turns the repressor on

(4)the rare sugar turns the repressor off

3.How is protein C regulated? (2 points)

(1)glucose turns the activator on

(2)glucose turns the activator off

(3)the rare sugar turns the activator on

(4)the rare sugar turns the activator off

4.How could you make the bacteria always use the rare sugar as the energy source even

in the presence of glucose? (8 points)

The simplest way: Change the promoter of fun3 gene to a strong promoter containing all the consensus sequence. Thus, fun3 gene is always highly expressed when rare sugar exists.

(其他的答案也可以酌情给分)

武汉大学分子生物学真题2001-2014

一.解释概念(20分,每个4分) 卫星DNA 复制体逆转座子反式激活因子衰减子与衰减作用 三、问答题(50分) 1. 说出双链DNA复制起始有关的五种重要的酶或蛋白并简述它们的功能。(15分) 2. 简述增强子的特点和性质及作用机制。(10分) 3. 简述真核RNA聚合酶II的转录起始复合物装配过程和转录起始(15分) 4. DNA限制性内切酶EcoRI是人们熟悉的常用内切酶,它是在大肠杆菌 (E.coli)R株中发现的,它被广泛用于分子克隆操作和DNA分析。pUC质粒是常用克隆载体之一,它的多克隆位点上有EcoRI、BamHI、KpnI、HindIII等酶切点。假如要你把一段由EcoRI切割产生的外源DN**段克隆到pUC质粒中,并把重组质粒转化大肠杆菌R株来扩增,已知条件是所用的R菌株中只有EcoRI一种限制性内切酶,你设计如何做才能确保成功?为什么?(10分) 武汉大学2002分子生物学 三.问答: 1.简述(或绘图说明)真核细胞RNA聚合酶II转录的起始需要哪些基本转录因子及其装配过程(15分) 2.简述(或绘图说明)色氨酸操纵子弱化的机制(15分) 3.在讨论基因家庭时经常提到胚胎、胎儿和成体形成的蛋白质,这些述语是指什么现象?可用什么术语来描述这一类基因家族(5分) 4. 你正在进行Southern blot分析,并刚刚完成凝胶电泳部分,下一步是将胶浸泡在NaOH溶液中使DNA变性为单链,为了节约时间,你跳过这一步,直接把DNA 从胶上转到硝酸纤维素膜上,你将标记好的探针与膜杂交,却发现放射自显影结果是一片空白,哪里错了呢?(5分)

一、下列名词翻译成中文,并简要解释 1、Domains and motifs 2、Alternative splicing 3、Reporter genes 4、The PCR cycle 5、Restriction mapping 6、Multiple cloning sites 7、DNA libraries 8、Proteomics 9、Replicon 10、Semi-conservative replication 二、简答题(共5题,每题8分,共40分) 1、请列举三种以上蛋白质纯化技术,并说明不同纯化技术的简单原理。 2、简述DNA损伤与DNA突变之间的区别与相互关系。 3、简述密码的简并性(degeneracy)和同义密码子(synonymous codon)及其在生物学上的重要性。 4、简述原核生物转录起始与转录终止过程中所涉及的主要蛋白质和核酸结构及其具体作用。 5、简述cDNA文库的构建过程。 三、论述题(共5题,1-4题每题15分,第5题10分,共70分) 1、人类基因组计划完成的社会意义和科学意义是什么? 2、什么是操纵子(operon)?试说明色氨酸操纵子(Trp operon)在原核基因表达调控中的调控机制和重要作用。 3、请简要解释顺式作用元件与反式作用因子,并举二例加以说明它们的相互作用方式。 4、试说明真核细胞与原核细胞在基因转录、翻译及DNA的空间结构方面存在的主要差异,表现在哪些方面? 5、限制性核酸内切酶有哪几种类型?哪一种类型的限制酶最适合于基因工程,为什么?请简要说明其理由。

商务英语泛读 期末考试试卷

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