1answer.
Ask question
Login Signup
Ask question
All categories
  • English
  • Mathematics
  • Social Studies
  • Business
  • History
  • Health
  • Geography
  • Biology
  • Physics
  • Chemistry
  • Computers and Technology
  • Arts
  • World Languages
  • Spanish
  • French
  • German
  • Advanced Placement (AP)
  • SAT
  • Medicine
  • Law
  • Engineering
Andru [333]
3 years ago
8

The MCB operon encodes the following four core proteins: MCB250, MCB251, MCB252 and MCB253. MCB354 is encoded by a separate gene

. A mutation occurs in the third gene of the operon (i.e., mcb252) resulting in a stop codon in the middle of its coding sequence. As described previously, this might result in a polar effect on the downstream gene (i.e., mcb253) involving Rho dependent termination. What are two possible ways that this nonsense mutation might result in a polar effect post-transcriptionally?
Biology
1 answer:
Sergeeva-Olga [200]3 years ago
8 0

Answer:

In one way, the existence of a nonsense mutation would lead to the generation of a premature termination codon that will be identified by the RNA polymerase as a termination sequence encouraged by the activity of Rho factor to dissociate ribosome, thus, discharging RNA polymerase and preventing further transcription mechanism making the transcription of the downstream sequence impossible.  

For the second way, there is a need to consider that the mechanism is taking place post-transcriptionally. Thus, the effects should be devised after transcription has taken place and the only fate lies in the mechanism encouraged by the RNA dependent RNA-polymerase. However, for this to take place, the event of genetic recombination can also be taken into account leading to the appearance of the faulty gene in the sequence. Apart from this, the open reading frame is required to be co-expressive that would be the most suitable factor, which determines whether the downstream sequences will be transcribed or not post nonsense mutation.  

However, the total change relies upon the fact that the mutation is taking place artificially or is induced naturally. One more thing to consider is that there is an existence of another gene known as MCB 354, which is encrypted by another gene and is probably monitored by another promoter sequence. Thus, co-expression would probably be the mechanism in terms of the rho-dependent termination.  

You might be interested in
What are three similarities between photosynthesis and respiration?
Mademuasel [1]
Ellular Respiration and Photosynthesis both have an ATP Synthase. These processes both have buildups of H+ and the ATP Synthase transports the hydrogen ions down the concentration gradient. This process is called Chemiosmosis.
<span>Similarities between Photosynthesis and Cellular Respiration.
</span><span>Cellular Respiration and Photosynthesis are both metabolic pathways. This means that the products created in Cellular Respiration are the reactants in Photosynthesis. While the products created in Photosynthesis are the reactants in Cellular Respiration. They are also metabolic pathways within themselves. In Photosynthesis, the products from the first phase (NADPH and ATP) are used in the second phase of Photosynthesis as a source of energy. In Cellular Respiration some products of glycolysis, intermediate step, Krebs Cycle are the reactants in Oxidation Phosphorylation. </span> 
7 0
3 years ago
What is pcr based genetic test?
Makovka662 [10]
It is polymerase chain reaction hope this helps
4 0
3 years ago
En que etapa de la meiosis se forma un nuevo nucleo
finlep [7]

<span>Estoy 50% seguro de que la respuesta es profase</span>
5 0
3 years ago
In a food chain, if an arrow points from a robin to a worm it means that...
statuscvo [17]

Answer:

The answer is A.

Explanation:

The arrows represents being eaten by other organisms.

(Correct me if I am wrong)

5 0
4 years ago
Read 2 more answers
What is the cause of the hydranencephaly? Select one: a. Aqueductal stenosis b. Subaranchoid stenosis c. Overproduction of CSF d
Dennis_Churaev [7]

Answer:

The correct answer is d.

Explanation:

Hydranencephaly is a rare congenital anomaly characterized by the absence and replacement of the cerebral hemispheres by cerebrospinal fluid and necrotic remains, with preservation of the membranes (leptomeninges), within a skull of normal capacity and shape. It is the most severe form of cortical destruction cerebral bilateral and is considered an extreme form of porencephaly (focal cystic cavity). It mainly affects the territory of the internal carotid artery and middle cerebral artery, with preservation of the territories supplied by the vertebrobasilar arteries. The most accepted etiology is carotid vascular insufficiency, due to multiple causes (bleeding, placental thromboembolism, arteritis, vascular malformations, among others).

5 0
3 years ago
Other questions:
  • Alice wants to find out whether her pet gecko finds its prey based on vision. She thinks that her gecko will more easily see the
    13·1 answer
  • How can you obtain a cells ratio of surface area to volume?
    14·2 answers
  • An organism that can manufacture its own food from inorganic substances. Select one: a. denitrifying bacteria b. herbivore c. om
    15·2 answers
  • In cattle, red coat color is co-dominant to white coat color. What could be the result of a cross between a RR male and a WW fem
    12·1 answer
  • Why some plants may benefit more than others to certain variable
    11·1 answer
  • What is a learned behavior?
    13·2 answers
  • Why is water necessary for living organisms?
    9·1 answer
  • How does cardiovascular system help the body maintain homeostasis?
    13·2 answers
  • Which of the following gets nutrients by absorbing molecules from other organsims through ita cell wall or cell membrane?
    8·1 answer
  • The fluidity of the cell membrane is
    13·1 answer
Add answer
Login
Not registered? Fast signup
Signup
Login Signup
Ask question!