Question 1

What is nonsense-mediated mRNA decay and why does it matter?

Accepted Answer

Nonsense-mediated mRNA decay (NMD) is a quality control pathway that detects and degrades mRNAs containing premature stop codons. When a ribosome encounters a stop codon before the final exon during test translation, NMD factors are recruited to degrade the faulty mRNA. This surveillance mechanism ensures only functional proteins are produced, selecting for genetic combinations that maintain proper cellular function.

Question 2

How do exon junction complexes help identify defective mRNAs?

Accepted Answer

Exon junction complexes (EJCs) bind to mRNA at each splice site during pre-mRNA processing. During test translation, the ribosome displaces EJCs as it moves along the mRNA. If a stop codon appears before the final EJC is removed, the bound EJC signals that the mRNA is defective, triggering NMD and recruitment of degradation machinery.

Question 3

What role do Upf proteins play in mRNA degradation?

Accepted Answer

Upf proteins (Upf1, Upf2, and Upf3) work collaboratively to recognize and degrade faulty mRNAs. Upf1 is an ATP-dependent RNA helicase that unwinds RNA, while Upf2 and Upf3 help discriminate between normal and defective mRNAs. Upf3 binds to exon junction complexes and recruits exonucleases that degrade the marked mRNA, ensuring regulated protein degradation of non-functional transcripts.

Question 4

How do nonsense mutations differ from normal stop codons?

Accepted Answer

Normal stop codons (UAA, UAG, UGA) appear in the final exon and terminate translation appropriately. Nonsense mutations create premature stop codons within the reading frame of earlier exons, causing incomplete polypeptide synthesis. These incomplete proteins are typically inactive, but nonsense suppressors—mutations in tRNA genes producing specialized suppressor tRNAs—can insert amino acids at premature termination sites to restore function.

Question 5

Why is NMD more frequently observed in organisms with longer introns?

Accepted Answer

Organisms with longer introns are more likely to have incompletely spliced mRNAs that retain nonsense codons in the reading frame. These defective transcripts escape normal processing and enter the cytosol, where the ribosome detects the premature stop codon during test translation. The longer intron regions increase the probability of splicing errors that generate these faulty mRNAs requiring NMD surveillance.

Question 6

What happens during the test translation phase of NMD?

Accepted Answer

Test translation occurs as the mRNA emerges from the nuclear pore, with a ribosome scanning the transcript to check for errors. During this phase, the ribosome displaces exon junction complexes as it translates. If the ribosome reaches a stop codon while EJCs remain bound downstream, translation terminates prematurely and the NMD response is activated to degrade the defective mRNA.

Question 7

How can suppressor tRNAs rescue genes with nonsense mutations?

Accepted Answer

Suppressor tRNAs are specialized transfer RNAs produced by mutations in tRNA genes. These tRNAs can recognize premature termination codons and insert amino acids at those positions instead of terminating translation. By allowing translation to continue past the nonsense mutation, suppressor tRNAs enable the ribosome to produce a complete, potentially functional polypeptide from genes that would otherwise be inactivated.

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