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Unit 11 Assignment C

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Unit 11 Assignment C: Explore the principles of inheritance and their application in predicting genetic traits

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Explore the principles of inheritance and their application in predicting genetic
traits:

Gregor Mendel created the law of segregation that says that when gametes form, two
alleles responsible for a trait either segregate or separate and this leads to a new zygote
formation. The law says that when a parent passes along genes to a gamete, only one
gene is passed on and the allocation is random. When gametes undergo maturity, they
combine with other alleles to form zygotes. This law makes sure that during
reproduction each allele could be inherited when there are two copies of said gene. In
sexual reproduction, parents pass down identical copies of DNA, 23 chromosomes.
When there is only one copy, it is haploid and when there are two gametes present it is
diploid, in humans this means 46 chromosomes. When creating this law, Mendel based
it on several beliefs. This includes; a gene can exist in more than one allelic form, when
gametes form the allele pair separates to form single alleles, one allele is dominant,
and one is recessive. Mendel also created the law of dominance which stated that in
heterozygous alleles, one trait will hide another trait. The key principle of this theory is
that dominant alleles are expressed in heterozygotes whereas recessive traits are only
expressed if there is two recessive alleles present.

An Overview On Law Of Segregation And Law Of Dominance

principle of segregation / law of segregation; Mendel's second law | Learn Science at
Scitable

12.3B: Mendel’s Law of Dominance - Biology LibreTexts

Variation occurs between all organisms; it is the differences that can occur in
phenotypes in a population. A phenotype is how the genotype is expressed so therefore
the observable physical characteristics in an organism. These include shape, size, hair
colour, eye colour etc. A genotypic variation is a genetic difference, and a phenotypic
variation is how the environmental conditions have caused the genotype to be
expressed.

https://studymind.co.uk/notes/variation-and-its-causes/

https://www.britannica.com/science/phenotype

A genetic cross is when two different organisms are intentionally made to sexually
reproduce, this leads to the fusion of gametes and passes along half of their genetic
information to their offspring. This is used to understand how genetic traits can be
passed down generations.

What is a Genetic Cross? Learn with Examples | Vaia

A monohybrid cross is a genetic cross between two individuals that have homozygous
genotypes. Homozygous genotypes are two identical alleles, for example they can be

, dominant or recessive. This is shown by two capital letters such as PP or two lowercase
letters such as pp. This can result in phenotypes thar are opposite. Geneticists utilise
the study of monohybrid crosses to examine heterozygous genes (two different) from
parents that are passed along to their homozygous offspring. It is responsible for the
inheritance of one gene.

Monohybrid Cross - Definition and Examples | Biology Dictionary

A dihybrid cross is a cross with two organisms that are both heterozygous for different
traits. In this instance, each of the parental organisms contain unique traits. The
parents have different alleles for the trait that we will be observing. For example, one
parent who is heterozygous dominant will the genotype YYRR and the other parent who
is heterozygous recessive will have the genotype yyrr.

Dihybrid Cross - Definition, Examples and Quiz | Biology Dictionary

A genotypic variation is caused due to a difference in the number or a change to the
chromosomal structure. They can also be caused by gene differences and mutations. A
phenotypic variation can be caused by several factors, such as the climate of the
individual, the food supply available to the individual. For example, someone genotype
could code for proteins that will make someone grow to be 6 feet tall, however, due to a
decreased food supply, their growth was stunted so they are now only 5 feet 6 inches.

There are types of variation among species. The first type of variation is discontinuous
variation, this is when there are specific classes among species, such as blood groups
in humans. There is only a certain amount of blood groups, due to the receptor proteins;
A, AB, O-, O+. Discontinuous variation has no intermediates; there is one single gene
that is involved.

Continuous variation is when there is not a specific class among the species due to
different phenotypic expressions, these can include hight, skin colouration and
personality. There is not one singular gene that is responsible for these characteristics,
there are several genes that consider environmental impacts.

Variation | Definition, Examples, & Facts | Britannica

Co dominance is a form of inheritance, it is when both alleles are expressed equally,
the heterozygotes express both alleles. This may occur in diseases such sickle cell
anaemia and cystic fibrosis. However, because the carriers of these diseases are
heterozygous, and they have one normal functioning allele so they can produce enough
of the protein to not suffer from symptoms.

Codominance | Definition & Examples - Lesson | Study.com

Incomplete dominance is when contrasting phenotypes are expressed in offspring, an
example of this is in flowers, one allele will code for red flowers and the other will code
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