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Index >> Monohybrid Crosses and Law of segregation>> Genetical Terminology

Genetical Terminology

Genetical Terminology
Any measurable characteristic or distinctive trait possessed by an organism is called phenotype of that organism. A phenotypic trait may be visible to eye, such as the colour of a flower or the texture of hair, or it may require special tests for its identification, as in the determiniation of the respiratory quotient or the serological test for blood type. Each phenotypic trait of an organism is caused and determined by at least two Mendelian factors which are now called genes. Out of these two genes, one gene has been derived from the maternal parent via the ovum and other gene from the paternal parent via the sperm during fertilization.  The genes may be defined as hereditary units which reside in a long DNA molecule (the main constituent molecule of chromosome) and contains coded instructions or informations for the production of proteins, the organic substances which ultimately cause and determine a phenotypic trait in a given environment.

It is customary in genetic studies to think of the phenotype as being the product of a reaction between its hereditary constitution or lenotype and the environment, according to the following scheme : Genetical Terminology
For example in honey bee Apis mellifera, the difference between the queen and the workers depend on nutritional differences and on pheromones, at the larval stage. Further, the flowers of hydrangea may be blue if grown in acid soil or pinkish if grown in alkaline soil, due to an interaction of gene products with the hydrogen-ion concentration (pH value) of their environment.
The genes are though stable and self replicating structures, but on certain rare occasions a change may occur simultaneously in them. This change is called a mutation. Mutation alters the coded informations of a gene and may result in the production of a defective protein or in the cessation of protein synthesis. The net result of a mutation is often seen as a change in the phenotypic trait.

Mutation may thus, change a gene into two or more alternative forms called allelomorphs or alleles. For example, the healthy people have a gene which specifies the normal protein structure of the red blood cell pigment called haemoglobin. Some anaemic individuals have an altered form of this gene, i.e., an allele, which makes a defective haemoglobin protein unable to carry the normal amount of oxygen to the body cells.
Further, each gene occupies specific position on a chromosome, called the gene locus (plural loci). All allelic forms of a gene are therefore found at corresponding positions on genetically similar (homologous) chromosomes. All the genes possessed by an individual constitute its genotype.

Genotypically, an organism may be either homozygous or heterozygous, for a particular phenotypic trait. A homozygous individual has identical alleles at both gene loci for a particular phenotypic trait. For example, a genetically pure tall pea plant has two alleles for tallness at both gene loci for the length of the stem. A homozygous individual (also called homozygote) is formed by the union of gametes carrying identical alleles and it produces only one kind of gametes during gametogenesis:
Homozygous Individual

1. Egg 2. Sperm 3. Fertilization

A heterozygous individual has different alleles for a particular phenotypic trait on both gene loci. For example, a F1 tall monohybrid of a cross of tall and dwarf pea plants is a. heterozygous individual because- it has one allele for tallness and another allele for dwarfness on the both gene loci for the length of the stem. An heterozygous individual is also called hybrid and it is formed by the union of gametes carrying different alleles. A hybrid or heterozygote produces different kinds of gametes:
Heterozygote Individual

1. Egg 2. Sperm 3. Fertilization
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