The right answer is inversion.
Inversion is a genetic mutation characterized by the end-to-end reversal of a portion of chromatid on a chromosome.
In other words, it is a double break then it is replaced after rotation of 180 ° of a chromosome segment (backward insertion).
We distinguish :
Paracentric inversions: The centromere in the chromosome is not included in the inversion.
Pericentric inversions: The centromere is included in the inversion which transforms a metacentric chromosome into an acrocentric chromosome.
I do not believe so because it is genetic, just you can't forever change a feature without plastic surgery or an accident, etc.
Answer:
Explanation:
If there are 5 genes, let us assume that they are in the alternative forms with 2 possible gets for each five... So we have
2 possible gametes for each five = 2 to the power of 5 = 32 gametes
Then genotypes = 3 to the power of 5 = 243
The same also for 10 genes
2 possible gametes for each 10 = 2 to the power of 10 = 1024 gametes
Then genotypes = 3 to the power of 10 = 59,049
The same also for 20 genes
2 possible gametes for each 20 = 2 to the power of 20= 1,048,576
Them genotypes = 3 to the power of 20 = 3,486,784,401
Answer:
The crust forms at the ridge and is carried away by the movement of the plate as new crust forms to take its place. The oceanic crust is youngest new a mid ocean ridge and oldest far away from it.
Explanation:
Answer:
they are evolutionary neutral
Explanation:
Transposons are genetic mobile elements that move into the genome by means of cut-paste and copy-paste mechanisms. In consequence, transposons are known to produce mutations in the inserted genomic sequences.
Non-coding DNA regions have been generally assumed to be evolutionary neutral, it means that they might resist genetic polymorphisms (such as, for example, those caused by the insertion of transposon elements) and don't have direct effects on the phenotype of the organism. However, it is important to note that recent evidence supports the idea that noncoding sequences play important regulatory roles, thereby mutations in these genomic regions may have a deleterious effect on the organism.
