TLS Online TPP Program

#Question id: 13091


To express a yeast gene in E. coli, your task is to design a strategy to insert the yeast gene into the bacterial plasmid. Below is a map of the area of the yeast genome surrounding the gene in which you are interested.
 
The distance between each tick mark placed on the line above is 100 bases in length
Below are the enzymes you can use, with their specific cut sites shown 5’-XXXXXX-3’ 3’-XXXXXX-5’
 
The plasmid is 5,000 bases long and the two farthest restriction enzyme sites are 200 bases apart. The plasmid has an ampicillin resistance gene somewhere on the plasmid distal from the restriction cut sites.
                              
You do the digestion of the insert and the vector and then ligate the two digestions together. You then transform the ligation into bacteria and select for ampicillin resistance. You get three colonies on your transformation plate. You isolate plasmid from each one and cut each plasmid with the enzyme XbaI. You then run your three digestions on an agarose gel and see the following patterns of bands. Describe what each plasmid actually was that was contained in each of the three colonies.
 
Which colony’s plasmid do you actually want to use for your studies?

#SCPH01 Biochemistry
  1. colony-1 because you want the bacterial promoter to drive transcription of the yeast gene in the correct orientation
  2. colony-2 because you want the bacterial promoter to drive transcription of the yeast gene in the correct orientation
  3. colony-3 because you want the bacterial promoter to drive transcription of the yeast gene in the correct orientation
  4. All colonies because the correct strand of DNA is used as a template in transcription.
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TLS Online TPP Program

#Question id: 2985

#I Life Science/ Life Sciences Group – I-V

Use the figure to answer the question below. The unlettered circle at the top of the figure shows a diploid nucleus with four chromosomes that have not yet replicated. There are two pairs of homologous chromosomes, one long and the other short. One haploid set is black, and the other is gray. The circles labeled A to E show various combinations of these chromosomes. What is the correct chromosomal condition for one daughter nucleus at telophase of mitosis? 

TLS Online TPP Program

#Question id: 2985

#SCPH06 I Botany

Use the figure to answer the question below. The unlettered circle at the top of the figure shows a diploid nucleus with four chromosomes that have not yet replicated. There are two pairs of homologous chromosomes, one long and the other short. One haploid set is black, and the other is gray. The circles labeled A to E show various combinations of these chromosomes. What is the correct chromosomal condition for one daughter nucleus at telophase of mitosis? 

TLS Online TPP Program

#Question id: 2986

#I Life Science/ Life Sciences Group – I-V

During ubiquitin-mediated protein degradation in various events of cell cycle, ubiquitin-protein ligases ubiquitinylate substrate proteins, marking them for degradation by proteasomes. Cyclins are degraded through the action of two different ubiquitin-protein ligases, SCF and the anaphase-promoting complex or cyclosome. Following statements are regarding to SCF and APC/C.

A. SCF controls the G1–S phase transition by degrading G1/S phase cyclins and, CDK inhibitory proteins.

B. APC/C degrades S phase and mitotic cyclins, thereby promoting the exit from mitosis.

C. SCF and APC/C are multi-subunit ubiquitin-protein ligases that belong to the RING finger family of ubiquitin protein ligases.

D. SCF and APC/C belong to the different ubiquitin-protein ligase family, their regulation is same.

E. SCF recognizes its substrates only when they are phosphorylated.

F. SCF and APC/C both recognizes its substrates only when they are phosphorylated.

Which of the following is incorrect?

TLS Online TPP Program

#Question id: 2986

#SCPH06 I Botany

During ubiquitin-mediated protein degradation in various events of cell cycle, ubiquitin-protein ligases ubiquitinylate substrate proteins, marking them for degradation by proteasomes. Cyclins are degraded through the action of two different ubiquitin-protein ligases, SCF and the anaphase-promoting complex or cyclosome. Following statements are regarding to SCF and APC/C.

A. SCF controls the G1–S phase transition by degrading G1/S phase cyclins and, CDK inhibitory proteins.

B. APC/C degrades S phase and mitotic cyclins, thereby promoting the exit from mitosis.

C. SCF and APC/C are multi-subunit ubiquitin-protein ligases that belong to the RING finger family of ubiquitin protein ligases.

D. SCF and APC/C belong to the different ubiquitin-protein ligase family, their regulation is same.

E. SCF recognizes its substrates only when they are phosphorylated.

F. SCF and APC/C both recognizes its substrates only when they are phosphorylated.

Which of the following is incorrect?

TLS Online TPP Program

#Question id: 2987

#I Life Science/ Life Sciences Group – I-V

Following statements are regarding the goals of gap phases.

(i) to prepare for the next phase of the cell cycle.

(ii) to check that the previous phase of the cell cycle has been completed appropriately.

(iii) to inhibits CDKs activity.

(iv) to enhance servillance mechanisms.

Which of the following is correct?

TLS Online TPP Program

#Question id: 2987

#SCPH06 I Botany

Following statements are regarding the goals of gap phases.

(i) to prepare for the next phase of the cell cycle.

(ii) to check that the previous phase of the cell cycle has been completed appropriately.

(iii) to inhibits CDKs activity.

(iv) to enhance servillance mechanisms.

Which of the following is correct?