Answer:
genomic imprinting
Explanation:
Genomic imprinting is a mechanism for regulating gene expression that allows expression of only one of the parental alleles, although both alleles are functional. Unlike most genes in which expression is biallelic, genes that are subjected to this mechanism (imprinted genes) have monoalelic expression; By definition, in an imprinted loci, only one allele is active (maternal or paternal), and the inactive is epigenetically marked by histonic modification and / or methylation of cytosines.
Genomic imprinting can cause some disturbances, among them Prader-Willi syndrome, which is a genetic disorder that involves a partial deletion of chromosome 15q on the paternal chromosome.
It has a charge shift, which basically means, since there are 2 charges, that it'll filp it's charge:
- If the atom had a positive charge, it'll become negative
- If the atom had a negative charge, it'll become positive
Hope it helped,
BioTeacher101
Explanation:
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Proteins can denature at extreme temperatures, or denature when inhibits are present. When this happens their functionality is dramatically reduced.
The answer is Genes on the same chromosome are sometimes inherited disparately. I had the exact same question and that was the answer hope this helped! Have a good day!
