Prader- Willi syndrome is a genetic disorder involving a partial deletion of chromosome 15q on the paternal chromosome. When both copies of a gene (or chromosome) are functional but only one is expressed, this is an example of __________ .
A) genomic imprinting
B) histone acetylation
C) X- inactivation
D) chromatin modifications
E) position effect variegation
Correct Answer:
Verified
Q7: You have identified a mutation in a
Q8: If you want to affect chromatin packaging,
Q9: Typically, acetylation of histone tails leads to_
Q10: Loss of Xist gene due to mutation
Q11: Which protein binds to the silencer sequence
Q13: Chromatin from two tissues, skin and liver,
Q14: Chromatin remodeling involves both sliding and relocating
Q15: dsRNA is detected and cleaved by?
A) RISC
B)
Q16: Enhancers and silencers are?
A) are proteins that
Q17: For the following gene, MspI and HpaII
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