Genetics: Dominant and Recessive Traits

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SUMMARY

The discussion centers on the expression of dominant and recessive alleles in genetics, specifically addressing whether both alleles are transcribed and translated. It is established that dominant alleles do not silence recessive alleles, and the expression of a gene depends on the biochemical function of the alleles involved. For instance, in cystic fibrosis, both alleles can be expressed, but the recessive allele produces a malfunctioning protein. Incomplete dominance is illustrated through the example of snapdragon flowers, where both alleles may or may not be expressed depending on their functionality.

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  • Understanding of dominant and recessive alleles
  • Knowledge of gene transcription and translation processes
  • Familiarity with incomplete dominance concepts
  • Basic genetics terminology, including alleles and mutations
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  • Research "Cystic Fibrosis CFTR protein function" for insights on allele expression
  • Study "Incomplete dominance in plant genetics" for examples beyond snapdragons
  • Explore "Genetic imprinting mechanisms" to understand advanced genetic concepts
  • Review "Haploinsufficiency in genetics" for implications of allele functionality
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I feel like I should know the answer to this, but I don't. Here is my question:

I understand that an individual has two copies of each gene, one maternal and one paternal. But if one is completely dominant over the other, will both gene copies be transcribed and translated, or only the one that is dominant?

And same for incomplete dominance, will both genes will be transcribed and translated, resulting in an intermediate phenotype?

Thanks!
 
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In general, dominant alleles do not silence the expression of recessive alleles. How exactly an allele functions as dominant or recessive depends on the exact biochemical function of the genes involved. Many dominant alleles code for a protein that causes a specific function and recessive alleles are loss-of-function mutatants. As long as you have one copy of the correctly functioning allele, the gene is still able to perform its function correctly, so the defect shows up only when both alleles of the gene are not functioning correctly.

Recessive alleles sometimes contain mutations that prevent expression of the protein. In these cases, the gene will be expressed from the dominant allele but not the recessive allele. This is not always the case, however. For example, in those heterozygous for cystic fibrosis, the CFTR protein is expressed from both the dominant non-disease allele and the recessive disease allele, but the protein produced from the disease allele does not fold properly and gets degraded. Even though ~ half of the CFTR protein gets degraded, the CFTR produced from the non-disease allele is sufficient to ensure correct function, so those heterozygous for the cystic fibrosis allele do not develop the condition.

Incomplete dominance can be tricky. The classic example is the color of snapdragon flowers with RR giving red flowers, Rr giving pink flowers, and rr giving white flowers. Here, I suspect the R allele encodes for the protein that produces the red pigment and the r allele contains a mutation that prevents correct expression of the red pigment-producing protein. In this case, only the R allele is correctly expressed. However, there are probably cases of incomplete dominance where both alleles are expressed.

Here's probably a good resources to read for more information: http://en.wikipedia.org/wiki/Haploinsufficiency

jedishrfu's post refers to a more advanced topic in genetics called imprinting, which occurs ins a some specialized cases.
 
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