WBR0099
| Author | [[PageAuthor::William J Gibson (Reviewed by Yazan Daaboul, M.D.)]] |
|---|---|
| Exam Type | ExamType::USMLE Step 1 |
| Main Category | MainCategory::Genetics |
| Sub Category | SubCategory::Musculoskeletal/Rheumatology |
| Prompt | [[Prompt::A 8-year-old boy is brought to the pediatrician's office by his mother for chronic weakness. She reports that her child started to have trouble running and rising from chairs at the age of 5. He has become progressively weaker over the past 3 years and now requires braces to walk. Physical examination is remarkable for proximal weakness of the upper and lower extremities. The pediatrician also notes atrophy of the gluteus maximus and accessory muscles of the pelvis, with unusually large calf muscles. The physician suspects a genetic disease and refers the patient to genetic testing. Which of the following mRNA sequences is most likely present in this patient?
Normal DNA Sequence:
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| Answer A | AnswerA::5'...GGC TAC GTA AAG AAG TCT...3' |
| Answer A Explanation | [[AnswerAExp::This sequence reflects a missense mutation, which is not usually a common cause of Duchenne muscular dystrophy.]] |
| Answer B | AnswerB::5'...GGT ACG TGA AGA AGA TCT...3' |
| Answer B Explanation | [[AnswerBExp::This sequence comprises two mutations: One mutation from 5'...GGC T to GGT...3' reflects a one base pair deletion; while the other is a one base pair insertion after 5'...AAG AAG T...3' to 5'...AAG AAG AT...3'. The first mutation disrupts the frame of the sequence whereas the second mutation restores it. The above sequence thus reflects 5 missense mutations with no nonsense mutations. The series of two mutations is extremely unlikely and does not commonly explain the genetic disorder observed in Duchenne muscular dystrophy.]] |
| Answer C | AnswerC::5'...GGC TAA GTG AAG AAG TCT...3' |
| Answer C Explanation | [[AnswerCExp::This mutation reflects the insertion of an inappropriate stop codon 5'...TAC to TAA...3'. mRNA transcription of this sequence will be: 5'...GGC UAA GUG AAG AAG UCU...3'. The second trinucleotide UAA is a stop codon, which does not correspond to any amino acid. It leads to the formation of a truncated dystrophin protein.]] |
| Answer D | AnswerD::5'...GGC TAC GTG ATG AAG TCT...3' |
| Answer D Explanation | [[AnswerDExp::This sequence reflects a missense mutation, which is not usually a cause of Duchenne muscular dystrophy.]] |
| Answer E | AnswerE::5'...GGC TAC GTG AAG AAG AAG...(x20)...TCT...3' |
| Answer E Explanation | [[AnswerEExp::This mutation reveals a trinucleotide repeat expansion. Generally, repeat expansions are identified among patients with Huntington’s disease (CAG), Fragile X syndrome (CGG), Friedreich ataxia (GAA), and myotonic dystrophy (CTG). Duchenne muscular dystrophy is not a trinucleotide repeat expansion disease.]] |
| Right Answer | RightAnswer::C |
| Explanation | [[Explanation::Duchenne muscular dystrophy (DMD) is a recessive X-linked genetic disease that affects 1 in 3500-6000 live male births. The disorder is caused by a mutation in the dystrophin gene, which is the largest human gene comprised of 2.6 million base pairs of DNA and 79 exons. The majority of dystrophin mutations are due to frameshift mutations by deletions or insertions, but point mutations have also been described among patients with DMD. Dystrophin gene normally encodes the dystrophin protein, a major structural protein that links the internal cytoskeleton of muscle cells to the extracellular matrix. Most patients with DMD lack any dystrophin protein.
The majority of patients with DMD are diagnosed at approximately the age of 5 years. Clinical features include delayed motor milestones, inability to run, jump, or physically compete with peers at school due to progressive weakness of the proximal muscles, such as the hip abductors and the quadriceps. Additionally, patients are unable to arise from the floor, showing the classical Gower's maneuver. On physical examination, patients typically have proximal muscle weakness with atrophy of large muscles, such as the gluteus maximus muscle, and pseudohypertrophy of the calves due to replacement of muscles by fibrofatty tissue. Most patients are wheelchair-bound by the age of 12-13, and die by the age of 18-20 years due to respiratory failure. The most likely mutation to cause DMD is a deletion/insertion that leads to frameshift error downstream by creating a stop codon. It is important to remember that DNA has 2 strands: 5' to 3' (sense strand) and a complementary 3' to 5' (anti-sense strand). The 3' to 5' DNA strand (anti-sense strand) is the one that is transcribed by mRNA; and mRNA is read from 5' to 3'. Accordingly, the mRNA will have a complementary sequence to the 3' to 5' antisense strand, but an identical sequence to the 5' to 3' sense strand, with the exception of having uracil (U) replacing every thymine (T). In humans, only 3 mRNA codons are stop codons: UAA, UGA, and UAG. Nowak KJ, Davies KE. Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment. EMBO Rep. 2004;5(9):872-6 First Aid 2014 page 89]] |
| Approved | Approved::Yes |
| Keyword | WBRKeyword::Muscle, WBRKeyword::Muscular Dystrophy, WBRKeyword::mutation, WBRKeyword::gene, WBRKeyword::nucleotide, WBRKeyword::genetics, WBRKeyword::weakness, WBRKeyword::Duchenne muscular dystrophy, WBRKeyword::Duchenne Muscular Dystrophy, WBRKeyword::frameshift mutation, WBRKeyword::frameshift, WBRKeyword::DNA, WBRKeyword::mrNA, WBRKeyword::RNA, WBRKeyword::template, WBRKeyword::strand, WBRKeyword::sense, WBRKeyword::antisense, WBRKeyword::antisense, WBRKeyword::DNA strand, WBRKeyword::mRNA strand, WBRKeyword::complement |
| Linked Question | Linked:: |
| Order in Linked Questions | LinkedOrder:: |