Concept of Genetics form four full notes

 

Concept of Genetics

The concept of Genetics

Explain the concept of the genetics

Genetics is a branch of biology which deals with the study of heredity and variations in organisms.

Heredity refers to the transmission of genetic information from one generation to another. That is, the passing on of features or characteristics from parents to offspring or progeny. In humans, for example, features such as hair colour and body shape of the parents can be passed on (inherited) to their children. In genetics, a feature that can be inherited by the offspring from the parent is known as a trait. Thus, features such as hair texture, hair colour, and skin colour are all traits.

The hereditary characteristics are passed on from parents to their offspring through distinct units called genes. Genes are hereditary materials or factors, which determine a specific characteristic or trait in an organism.

Variations are the observable differences in organisms of the same species. Living things arise from other living things of the same species through reproduction. However, organisms show a great number of variations. No two organisms are exactly the same. The variations may be due to mutations of genetic material (DNA) caused by x-rays, gamma rays, ultra radiations or radioactive elements. Variations may also occur during gamete formation and combination of gametes at fertilization.

Genetics, therefore, attempts to explain either how organisms do resemble their parents in certain features or differ from their parents in other features.

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Common terms used in Genetics

State common terms used in genetics

In genetics, there are several terms that are often used to describe different genetic features, variations or phenomena. Defined below are some of the common terms used in genetics.

a.     F1 generation: The first filial generation arising from the crossing of two pure breeds.

b.     F2 generation: The generation obtained by crossing individuals of the F1 generation.

c.     Genotype: The genetic makeup or constitution of an organism, which is responsible for certain physical traits.

d.     Phenotype: The outward appearance of an organism determined by a gene.

e.     Haploidy (n): Having one set of unpaired chromosomes in the nucleus.

f.      Diploidy (2n): Having two sets of homologous (similar) chromosomes in the nucleus.

g.     Alleles: Different forms of the same gene occupying the same position on a chromosome, for example T or t for height.

h.     Homozygosity: The state of possessing two identical forms (alleles) of a particular gene, one inherited from each parent, for example tt, TT BB or bb.

i.       Heterozygosity: The state of possessing two different alleles of a particular gene at one or more corresponding chromosomal loci, one inherited from each parent, for example Tt or Bb.

j.       Dominance: A relationship between alleles of one gene, in which the effect on phenotype of one allele masks the contribution of a second allele at the same locus. The first allele is dominant and the second allele is recessive. For example, in height, both TT and Tt express tallness. Here, the contribution of “t” allele to the phenotype is masked by “T” allele.

k.     Recessiveness: A condition where an allele can only express itself in a homozygous form, for example tt for dwarfness.

l.       Mutation: A sudden, random change in the genetic make up of a cell, causing it and all cells derived from it to differ from normal cells.

m.   Mutagen: An agent capable of increasing the rate of mutation in an organism, such as formaldehyde or nitrous acid.

n.     Selfing: Crossing offspring of the same pair of parents. For example, the crossing of offspring of F1 generation to produce F2 (F1×F1 = F2) is called selfing.

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Genetics Materials

The concept of Genetics Materials

Explain the concept of genetics Materials

Hereditory characteristics are passed from parents to their offspring through distinct units called genes.There are a lot of genes in an organism’s body. Genes are arranged in a linear manner, making chromosomes.

Chromosomes are thread like structures found in the nuclei of all body cells. Gene is made up of chemical substances called Nucleic acid.

There are two types of nucleic acids found in cells, these are:

1.     Deoxyribonucleic acid (DNA)

2.     Ribonucleic acid (RNA)

These acids are made up of building blocks called nucleotides. Each nucleotide consists of three molecules linked together, that is a pentose sugar, phosphoric acid and organic base.

 


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