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In eukaryotes, premRNA splicing by the spliceosome occurs only in the nucleus and translation of mRNAs occurs only in the cytosol. Why might the separation of these two activities into different cellular compartments be important?

Short Answer

Expert verified
Separating splicing and translation into different compartments ensures correct mRNA processing and quality control, preventing harmful protein production.

Step by step solution

01

Understand the Basics of Splicing and Translation

In eukaryotic cells, pre-mRNA splicing occurs in the nucleus, while translation occurs in the cytosol. Splicing involves removing introns from pre-mRNA to produce mature mRNA. Translation is the process where ribosomes synthesize proteins using the mature mRNA as a template.
02

Consider the Advantages of Compartmentalization

Having splicing and translation in separate compartments prevents premature translation of unprocessed mRNA. It ensures that only mature mRNA, free of introns, is exported to the cytosol for translation, reducing the risk of producing non-functional or harmful proteins.
03

Explore Error Prevention

The separation into different cellular compartments acts as a quality control mechanism. Mistakes in splicing could lead to improper protein synthesis if translation happened in the same compartment. Thus, the nucleus provides a safe environment to refine and perfect the mRNA before it reaches the ribosomes.
04

Identify the Regulatory Benefits

This separation allows for complex regulation of gene expression. The nucleus not only prepares the mRNA by splicing but also involves regulation through other modifications like capping and polyadenylation, which do not interfere with translation processes, thus providing a more controlled output.
05

Summarize the Importance of Spatial Separation

The physical separation between the processes of splicing and translation ensures that mRNA is correctly processed and regulated before protein synthesis, which is critical for maintaining cellular function and protecting the cell from potential errors in protein production.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

spliceosome function
In eukaryotic cells, the spliceosome plays a crucial role in the processing of pre-mRNA. This complex of proteins and RNA operates in the nucleus and is responsible for removing non-coding regions known as introns from the pre-mRNA. The remaining sequences, called exons, are joined together to form a mature mRNA molecule. The ability of the spliceosome to recognize and accurately remove introns is crucial for the correct expression of genes. A mistake in splicing can lead to errors in mRNA, potentially resulting in faulty proteins that could disrupt cell function. Understanding the precise mechanics of the spliceosome helps underline its importance in eukaryotic cells. By ensuring that only mature and properly configured mRNA is exported from the nucleus, the spliceosome minimizes the risk of errors during protein synthesis.
mRNA translation
Translation is the process by which the ribosomes in the cytosol synthesize proteins. It uses the mature mRNA as a template to guide the assembly of amino acids into a polypeptide chain. This process is extremely precise and requires a properly formed mRNA to ensure that the correct protein is synthesized. During translation:
  • Ribosomes read the sequence of the mRNA in groups of three bases at a time, known as codons.
  • Each codon corresponds to a specific amino acid or a stop signal for protein synthesis.
By occurring in the cytosol, translation is kept separate from processes that occur in the nucleus, like splicing. This spatial separation ensures only mature, error-free mRNA is translated, reducing the potential for spurious or non-functional proteins.
cellular compartmentalization
Cellular compartmentalization refers to the segregation of cellular processes into distinct areas within a cell. This organization is crucial for eukaryotic cells as it allows for increased efficiency and regulation. The benefit of having splicing occur in the nucleus and translation in the cytosol includes:
  • Protection from premature translation of unprocessed mRNA.
  • Ensuring error checking happens before mRNA reaches the ribosomes.
This physical separation acts as a quality control step that prevents translation of defective mRNA, which could lead to harmful protein formation. Thus, compartmentalization supports a reliable and efficient gene expression process.
gene expression regulation
Gene expression regulation involves various mechanisms that cells use to increase or decrease the production of specific gene products (protein or RNA). This regulation is vital for cellular function, development, and adaptability. Within the nucleus:
  • Splicing alters gene expression by enabling the production of different protein variants from a single gene.
  • Additional modifications, such as capping and polyadenylation, help regulate stability and export of mRNA to the cytosol.
By orchestrating a series of checks and modifications in the nucleus, cells can finely tune the amount and type of proteins produced, responding better to cellular signals and environmental conditions. Ultimately, regulating gene expression through these nuclear processes contributes to the overall efficiency and adaptability of cellular operations.

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Most popular questions from this chapter

Predict the likely effects of a mutation in the sequence \(\left(5^{\prime}\right)\) AAUAAA in a eukaryotic mRNA transcript.

The RNA genome of phage \(Q \beta\) is the nontemplate strand, or coding strand, and when introduced into the cell, it functions as an mRNA. Suppose the RNA replicase of phage \(\mathrm{Q} \beta\) synthesized primarily template-strand RNA and uniquely incorporated this, rather than nontemplate strands, into the viral particles. What would be the fate of the template strands when they entered a new cell? What enzyme would have to be included in the viral particles for successful invasion of a host cell?

The practical limit for the number of different RNA sequences that can be screened in a SELEX experiment is \(10^{15}\). a. Suppose you are working with oligonucleotides that are 36 nucleotides long. How many sequences exist in a randomized pool containing every sequence possible? b. What percentage of these can a SELEX experiment screen? c. Suppose you wish to select an RNA molecule that catalyzes the hydrolysis of a particular ester. From what you know about catalysis, propose a SELEX strategy that might allow you to select the appropriate catalyst.

DNA polymerases are capable of editing and error correction, whereas the capacity for error correction in RNA polymerases seems to be limited. Given that a single base error in either replication or transcription can lead to an error in protein synthesis, suggest a possible biological explanation for this difference.

The death cap mushroom, Amanita phalloides, contains several dangerous substances, including the lethal \(a\)-amanitin. This toxin blocks RNA elongation in consumers of the mushroom by binding to eukaryotic RNA polymerase II with very high affinity; it is deadly in concentrations as low as \(10^{-8}\) ?. The initial reaction to ingestion of the mushroom is gastrointestinal distress (caused by some of the other toxins). These symptoms disappear, but about 48 hours later, the mushroom-eater dies, usually from liver dysfunction. Speculate on why it takes this long for \(a\)-amanitin to kill.

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