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Gene Repression in Eukaryotes Explain why repression of a eukaryotic gene by an RNA might be more efficient than repression by a protein repressor.

Short Answer

Expert verified
RNA-mediated repression is often more efficient due to its direct, sequence-specific action on mRNA.

Step by step solution

01

Understand RNA-mediated Gene Repression

RNA-mediated gene repression in eukaryotes often involves mechanisms such as RNA interference (RNAi) where small RNA molecules, like siRNA or miRNA, can bind to mRNA transcripts and prevent their translation into proteins. This process can degrade the mRNA or block the ribosome from translating it.
02

Analyze Efficiency of RNA

RNA molecules can act directly on the mRNA, potentially in a more targeted and sequence-specific manner. Since they can bind to multiple mRNA transcripts, they may prevent the translation of these transcripts simultaneously, maximizing their repressive effect.
03

Compare with Protein Repressors

Protein repressors usually bind to DNA or to other proteins to inhibit gene expression. This involves more steps: synthesis of the repressor protein, its transport and binding to the appropriate site on DNA or interaction with transcription factors. These steps can be resource and time-intensive.
04

Conclusion on Efficiency

RNA can act more immediately and efficiently since it operates at the mRNA level after transcription has occurred. This circumvents the need for additional proteins and interactions, reducing the complexity and time required for gene repression.

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Key Concepts

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

RNA interference
RNA interference, or RNAi, is a biological process in eukaryotic cells that allows RNA molecules to inhibit gene expression or translation. It is a vital mechanism employed most often as a method of controlling the expression of genes. Normally, this process involves small RNA molecules, such as siRNA (small interfering RNA) or miRNA (microRNA), that zero in on specific mRNA molecules. By binding to these mRNA molecules, RNAi can interfere with their function in the cell, typically leading to the degradation of the mRNA or hindrance of its translation into proteins. The beauty of RNAi lies in its precision, targeting specific sequences in mRNA and potentially neutralizing multiple copies of mRNA simultaneously due to shared sequences. This makes RNA interference an efficient tool for gene suppression, as it operates after transcription, meaning that it circumvents many of the more resource-intensive steps that proteins face.
siRNA
Small interfering RNAs (siRNAs) are pivotal to the mechanism of RNA interference. These are short, double-stranded RNA fragments, typically about 20-25 nucleotides in length. Their principal action in the process of gene repression is to specifically degrade mRNA molecules that are perfectly complementary to them. When siRNAs are introduced into the cell, they are integrated into the RNA-induced silencing complex (RISC). Once part of the RISC, they guide the complex to bind to corresponding mRNA targets. This binding triggers the slicing and degradation of the mRNA, effectively preventing it from being translated into a protein. This method is not only effective but highly specific, as the siRNA requires exact sequence matching to the mRNA target. This specificity helps scientists prevent unintended off-target effects thereby offering precise control in gene silencing applications.
miRNA
MicroRNAs (miRNAs) are an essential component of the RNA interference system. Unlike siRNAs, miRNAs are single-stranded and typically originate from segments of RNA that form hairpin structures. These molecules are not completely complementary to their target mRNAs. Instead, they usually have an imperfect match, allowing them to regulate the expression of multiple genes post-transcriptionally. Most miRNAs act by binding to target mRNAs at the 3' untranslated regions (UTRs) and preventing their translation into proteins. This suppression may not lead to mRNA degradation but often results in reduced levels of the encoded protein. miRNAs are involved in various cellular processes, including differentiation, proliferation, and apoptosis. Their less stringent binding requirements enable them to interact with multiple mRNAs and exert a broad influence across the genome, providing a flexible yet powerful approach to gene regulation.
Protein Repressors
Protein repressors are molecules that control gene expression by binding to specific sequences in DNA. These proteins act by either blocking the progression of RNA polymerase along the DNA strand or interacting with other proteins involved in the transcription process. Unlike RNA interference, repression by proteins typically occurs at the level of transcription. This means the repressor proteins need to be synthesized first, which requires their own mRNA and translation process. Once synthesized, they must be transported to the nucleus to perform their function, possibly having to bind DNA at multiple sites to repress transcription effectively. This multistep process can be resource and time-consuming. The mechanism of protein repression is more complex and may involve additional interactions with co-repressors or other transcription factors. This often makes RNA-based repression more appealing due to its relative simplicity and efficiency compared to the transcriptional inhibition model by protein repressors.

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Most popular questions from this chapter

Transcription Attenuation How would each manipulation of the leader region of the \(\operatorname{trp}\) mRNA affect transcription of the \(E\). coli trp operon? a. Increasing the distance (number of bases) between the leader peptide gene and sequence 2 b. Increasing the distance between sequences 2 and 3 c. Removing sequence 4 d. Changing the two Trp codons in the leader peptide gene to His codons e. Eliminating the ribosome-binding site for the gene that encodes the leader peptide f. Changing several nucleotides in sequence 3 so that it can base-pair with sequence 4 but not with sequence 2

Regulation by Recombination In the phase variation system of Salmonella, what would happen to the cell if the Hin recombinase became more active and promoted recombination (DNA inversion) several times in each cell generation?

Repressor Concentration in \(\boldsymbol{E}\). coli The dissociation constant for a particular repressor-operator complex is very low, about \(10^{-13}\) M. An \(E\). coli cell (volume \(2 \times 10^{-12} \mathrm{~mL}\) ) contains 10 copies of the repressor. Calculate the cellular concentration of the repressor protein. How does this value compare with the dissociation constant of the repressoroperator complex? What is the significance of this answer?

Specific DNA Binding by Regulatory Proteins A typical bacterial repressor protein discriminates between its specific DNA-binding site (operator) and nonspecific DNA by a factor of \(10^{4}\) to \(10^{6}\). About 10 molecules of repressor per cell are sufficient to ensure a high level of repression. Assume that a very similar repressor existed in a human cell, with a similar specificity for its binding site. How many copies of the repressor would a human cell require to elicit a level of repression similar to that in the bacterial cell? (Hint: The \(E\). coli genome contains about \(4.6\) million bp; the human haploid genome has about \(3.2\) billion bp.)

Negative Regulation Describe the probable effects on gene expression in the lac operon of each mutation: a. Mutation in the lac operator that deletes most of \(\mathrm{O}_{1}\) b. Mutation in the lacI gene that eliminates binding of repressor to operator c. Mutation in the promoter near position \(-10\) that increases its similarity to the \(E\). coli consensus sequence d. Mutation in the lacI gene that eliminates binding of repressor to lactose e. Mutation in the promoter near position \(-10\) that decreases its similarity to the \(E\). coli consensus sequence

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