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andrew-mc [135]
3 years ago
14

The original source of new alleles, upon which selection operates, is mutation, a random event that occurs without regard to sel

ectional value in the organism. Although many model organisms have been used to study mutational events in populations, some investigators have developed abiotic molecular models. Soll et al. (2006. Genetics 175: 267-275) examined one such model to study the relationship between both deleterious and advantageous mutations and population size in a ligase molecule composed of RNA (a ribozyme). Soll found that the smaller the population of molecules, the more likely it was that not only deleterious mutations but also advantageous mutations would disappear. Why would population size influence the survival of both types of mutations (deleterious and advantageous) in populations
Biology
1 answer:
maria [59]3 years ago
8 0

Answer:

Sampling error may allow fixation of one form and the elimination of others in a small population.

Explanation:

It can be seen that in case of a small population size, there are high chances of the elimination or the fixation of the allele in the population when compared to the large population size. Also sampling errors are found in case of small population size that leads to the enhancement of the chances for fixation and also for the elimination of the allele. This large size population doe not have much effect. The random fixation of the either selective allele or the elimination of the disadvantageous allele occurs due to the genetic drift.

SO in order for the population size influenced the survival of both types of mutations , the sampling error may be allowed for the fixation of one of the form and the elimination of the other forms in the small population size.

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Complete question:

You will find the pedigree in the attached files

Answer:

The correct option is C) <em>maternal mitochondrial mutations are inherited by </em><u><em>all of a mother's offspring</em></u><em>.</em>

Explanation:  

Mitochondrial inheritance is one of the ways in which a disease or a trait might be inherited from the maternal line.

Most of the DNI is located in the nucleus, but there is also DNI in mitochondria. Sperm cells hardly carry mitochondria, so mitochondrial DNI is mostly inherited from the maternal side. If there exists any mutation in this DNI, the whole progeny of the mutated woman will be affected, as they will get the mother´s mitochondria carrying the mutation. On the contrary, if there is a man affected by a disease caused by a mutation in mitochondrial DNI, non of their descendants will get the disease.

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