突变与变异解读
引入| English | 释义 | 拼音 |
|---|---|---|
| variant of uncertain significance | 意义未明变异 | yì yì wèi míng biàn yì |
| synonymous | 同义 | tóng yì |
| missense | 错义 | cuò yì |
| nonsense | 无义 | wú yì |
| frameshift/ˈfreɪmʃɪft/ | 移码 | yí mǎ |
| splice-site | 剪接位点 | jiǎn jiē wèi diǎn |
| copy number variants | 拷贝数变异 | kǎo bèi shù biàn yì |
| haploinsufficiency | 单倍剂量不足 | dān bèi jì liàng bù zú |
| dominant negative | 显性负效应 | xiǎn xìng fù xiào yìng |
"Variant of uncertain significance"
- A genetic report names a single changed letter and adds four words: of uncertain significance. A family now has to decide what to do with that.
- Interpreting variants is the daily work of medical genetics: a graded chain of evidence, not a yes or no.
Single-letter changes
- A synonymous 同义 variant changes a codon but not the amino acid. A missense 错义 variant swaps one amino acid for another.
- A nonsense 无义 variant creates an early stop codon, so the protein is cut short or the message is destroyed: usually serious.
A single-letter change turns a codon into a stop codon. What type of variant is it?
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A new stop codon cuts the protein short. A frameshift needs an insertion or deletion.
Bigger changes
- A frameshift 移码 is an insertion or deletion whose length is not a multiple of 3: every codon after it is misread. A splice-site 剪接位点 variant changes how exons are joined.
- Copy number variants 拷贝数变异 (CNVs) delete or duplicate whole exons or genes.
Match each variant type to its effect.
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The type predicts how badly the protein is damaged.
Six bases are deleted from a coding exon. How many amino acids are lost, assuming the frame is kept?
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6 ÷ 3 = 2 codons. Because 6 is a multiple of 3, the frame is kept.
Deleting 4 bases from a coding exon shifts the reading frame.
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4 is not a multiple of 3, so every codon after the deletion is read in the wrong frame.
Five verdicts
- Laboratories place each variant in one of five tiers: pathogenic, likely pathogenic, variant of uncertain significance 意义未明变异 (VUS), likely benign and benign.
- The evidence: how common it is in healthy people, computer predictions, laboratory tests of function, whether it tracks the disease in the family, and how well the gene is linked to the disease.
Put the five verdicts in order, from most to least likely to cause disease.
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The VUS sits in the middle, where the evidence points neither way.
Frequency comes first
- A variant common in healthy people cannot cause a rare, severe, early disease. Population databases such as gnomAD are checked before anything else.
- A variant predicted to be "damaging" but carried by 1% of healthy people is usually harmless background.
The gene's mechanism decides which variants count
- If one working copy is not enough, haploinsufficiency 单倍剂量不足, then truncating variants (nonsense, frameshift) cause disease. PAX6 in aniridia is an example.
- If a faulty protein spoils its normal partner, a dominant negative 显性负效应 effect, missense variants matter more. In a recessive gene, one variant makes a healthy carrier.
Worked example: the frequency check
- (Fictional) A dominant disease affects 1 person in 10 000; a variant is carried by 1 person in 100.
- Even if this variant caused every case, only $\dfrac{1/10\,000}{1/100} = \dfrac{1}{100}$ of carriers could be affected. It cannot be a fully penetrant cause, whatever the computer predicts.
A dominant disease affects 1 person in 20 000, and a variant is carried by 1 person in 200. Even if the variant caused every case, at most what percentage of its carriers could be affected?
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(1/20 000) ÷ (1/200) = 1/100 = 1%, far too common to be a fully penetrant cause.
Worked example: the VUS conversation
- (Fictional) A missense VUS in a breast-cancer gene is found in a woman with breast cancer. It is not treated as pathogenic, and her relatives are not tested for it.
- It may be reclassified later, if it is found to track the disease in families or appears in many more patients. The plain sentence: "We found a spelling change; we do not yet know whether it matters."
What is the right response to a VUS in a breast-cancer gene?
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A VUS is unknown. Decisions rest on the personal and family history until new evidence reclassifies the variant.
Three common slips
- "A VUS is probably pathogenic." It is explicitly unknown, and acting on it can mislead a whole family.
- "Predicted damaging means disease-causing." Prediction is weak evidence; frequency and family data count more.
- "Every deletion shifts the frame." A deletion of 3 or 6 bases removes amino acids but keeps the frame.
Recap
- Variant types: synonymous, missense, nonsense, frameshift, splice-site and CNV.
- Five tiers, from benign to pathogenic; a VUS stays a VUS until new evidence moves it.
- Frequency is the first filter, and the gene's mechanism decides which variant types count.