Suppose the mRNA being degraded in Figure 18.14 coded for a protein that promotes cell division in a multi-cellular organism. What would happen if a mutation disabled the gene for the miRNA that triggers this degradation?

Short Answer

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The defective miRNA (microRNAs) that triggers the degradation of a protein involved in the promotion of cell division would cause inappropriate division of cells. This can lead to uncontrolled growth of cells in the absence of proper cell division, leading to cancer development.

Step by step solution

01

Role of miRNA

miRNA are small single-stranded RNA (ribonucleic acid) molecules that are approximately 22 base pairs in length. These are produced from mRNA molecules by the action of cellular enzymes.

The function of the miRNA molecule is to base-pair with target mRNA and cause its degradation.

02

Mutation and development of cancer

Any change in the nucleotide sequence in the DNA (deoxyribonucleic acid) is a mutation. Thus, the mutation affects and disables the gene. The disabled gene produces a defective or malfunctioning protein or a molecule.

The defective protein or molecule affects the functioning of the cell. As a result, mutations affect the proper functioning of the organisms and are involved in the development of cancer.

03

Effect of disabled miRNA on degradation

mRNA synthesized in the cell would be translated to a protein that is involved in cell division. However, when a defective miRNA is produced due to mutation, the miRNA would not base-pair with the target mRNA and would not be able to cause its degradation.

If the miRNA does not base-pair with the target mRNA, the mRNA would not be degraded. This would lead to the production of a protein that would continue to promote cell division.

As a result, unchecked cell division leads to the formation of a clump of cells called tumors that would ultimately lead to cancer development.

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Most popular questions from this chapter

Cell differentiation always involves

(A) transcription of the myoD gene.

(B) the movement of cells.

(C) the production of tissue-specific factors

(D) the selection loss of certain genes from the genome.

Which of the following statements about the DNA in one of your brain cells is true?

(A) Most of the DNA codes for protein.

(B) The majority of genes are likely to be transcribed.

(C) It is the same as the DNA in one of your liver cells.

(D) Each gene lies immediately adjacent to an enhancer.

In Figure 18.17b, the lower cell is synthesizing signaling molecules, whereas the upper cell is expressing receptors for these molecules. In terms of gene regulation and cytoplasmic determinants, explain how these cells came to synthesize different molecules.

In general, what are the effects of histone acetylation and DNA methylation on gene expression?

The diagram below five genes, including their enhancers, from the genome of a certain species. Imagine that pink, blue, green, black, grey and dark blue activator proteins exist that can bind to the approximately colour-coded control elements in the enhancers of these genes.

(a) Draw an X above enhancer elements (of all the genes) that would have activators bound in a cell where only gene five is transcribed. Identify which coloured activators would be present.

(b) Draw a dot above all enhancer elements that would have activators bound in a cell where the green, blue, and yellow activators are present. Identify which gene(s) would be transcribed.

(c) Imagine that genes 1, 2, and 4 codes for nerve-specific proteins, and genes 3 and 5 are skin-specific. Identify which activators would have to be present in each cell type to ensure transcription of the appropriate genes.

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