Biology, asked by binitabhattarai962, 8 months ago

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Answers

Answered by annimalik69
0

AIn biology, a gene is a section of DNA that encodes a trait. The precise arrangement of nucleotides (each composed of a phosphate group, sugar and a base) in a gene can differ between copies of the same gene. Therefore, a gene can exist in different forms across organisms. These different forms are known as alleles. The exact fixed position on the chromosome that contains a particular gene is known as a locus.

In biology, a gene is a section of DNA that encodes a trait. The precise arrangement of nucleotides (each composed of a phosphate group, sugar and a base) in a gene can differ between copies of the same gene. Therefore, a gene can exist in different forms across organisms. These different forms are known as alleles. The exact fixed position on the chromosome that contains a particular gene is known as a locus.A diploid organism either inherits two copies of the same allele or one copy of two different alleles from their parents. If an individual inherits two identical alleles, their genotype is said to be homozygous at that locus.

Answered by nithra
0

Answer:

What is the definition of a genotype?

In biology, a gene is a section of DNA that encodes a trait. The precise arrangement of nucleotides (each composed of a phosphate group, sugar and a base) in a gene can differ between copies of the same gene. Therefore, a gene can exist in different forms across organisms. These different forms are known as alleles. The exact fixed position on the chromosome that contains a particular gene is known as a locus.

A diploid organism either inherits two copies of the same allele or one copy of two different alleles from their parents. If an individual inherits two identical alleles, their genotype is said to be homozygous at that locus.

However, if they possess two different alleles, their genotype is classed as heterozygous for that locus. Alleles of the same gene are either autosomal dominant or recessive. An autosomal dominant allele will always be preferentially expressed over a recessive allele.

The subsequent combination of alleles that an individual possesses for a specific gene is their genotype.

Genotype examples

Let’s look at a classic example – eye color.

A gene encodes eye color.

In this example, the allele is either brown, or blue, with one inherited from the mother, and the other inherited from the father.

The brown allele is dominant (B), and the blue allele is recessive (b). If the child inherits two different alleles (heterozygous) then they will have brown eyes. For the child to have blue eyes, they must be homozygous for the blue eye allele.

Image of brown and blue eyes that shows how eye color is inherited.

Figure 1: Inheritance chart detailing how an individual may inherit blue or brown eyes depending on the alleles carried by their parents, with the brown eye color allele being dominant and the blue eye color allele being recessive.

Other examples of genotype include:

Hair color

Height

Shoe size

What is the definition of a phenotype?

The sum of an organism’s observable characteristics is their phenotype. A key difference between phenotype and genotype is that, whilst genotype is inherited from an organism’s parents, the phenotype is not.

Whilst a phenotype is influenced the genotype, genotype does not equal phenotype. The phenotype is influenced by the genotype and factors including:

Epigenetic modifications

Environmental and lifestyle factors

Flamingos eating fish out of basket and changing color.

Figure 2: Flamingos are naturally white in color, it is only the pigments in the organisms that they eat that cause them to turn vibrantly pink.

Phenotype examples

Environmental factors that may influence the phenotype include nutrition, temperature, humidity and stress. Flamingos are a classic example of how the environment influences the phenotype. Whilst renowned for being vibrantly pink, their natural color is white – the pink color is caused by pigments in the organisms in their diet.

A second example is an individual's skin color. Our genes control the amount and type of melanin that we produce, however, exposure to UV light in sunny climates causes the darkening of existing melanin and encourages increased melanogenesis and thus darker skin.

Genotype vs phenotype: observing

Observing the phenotype is simple – we take a look at an organism’s outward features and characteristics, and form conclusions about them. Observing the genotype, however, is a little more complex.

Genotyping is the process by which differences in the genotype of an individual are analyzed using biological assays. The data obtained can then be compared against either a second individual’s sequence, or a database of sequences.

Previously, genotyping would enable only partial sequences to be obtained. Now, thanks to major technological advances in recent years, state-of-the-art whole genome sequencing.

A workflow showing the steps of whole genome sequencingFigure 3: A workflow depicting the various steps of whole genome sequencing (WGS).

(WGS) allows entire sequences to be obtained. An efficient process that is increasingly affordable, WGS involves using high-throughput sequencing techniques such as single-molecule real-time (SMRT) sequencing to identify the raw sequence of nucleotides constituting an organism’s DNA.

WGS is not the only way to analyze an organism’s genome - a variety of methods are available.

Genotyping Techniques:

• PCR

• DNA Microarray

• Allele-specific Oligonucleotide (ASO) Probes

• DNA Hybridization

Explanation:

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