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Understanding Genetic Inheritance Basics

Inheritance is the process of passing genetic information from parents to offspring, with traits determined by genes located on chromosomes. DNA contains instructions for protein synthesis, which in turn influences the traits of organisms. Genotypes, which can be homozygous or heterozygous, determine the expression of traits through dominant and recessive alleles.

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0% found this document useful (0 votes)
10 views13 pages

Understanding Genetic Inheritance Basics

Inheritance is the process of passing genetic information from parents to offspring, with traits determined by genes located on chromosomes. DNA contains instructions for protein synthesis, which in turn influences the traits of organisms. Genotypes, which can be homozygous or heterozygous, determine the expression of traits through dominant and recessive alleles.

Uploaded by

Naveed Ullah
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© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PPTX, PDF, TXT or read online on Scribd

Inheritance

Inheritance refers to the process by which


genetic information, encoded in DNA, is
passed from one generation to the next.
Introduction To Genetics
Genetics is the branch of biology that studies
inheritance.
Inheritance refers to the transmission of
characteristics from parents to offspring.
These characteristics are called traits, such as
height, eye color, and intelligence.
Parents pass characteristics to their offspring
through gene transmission.
During fertilization, an equal number of
chromosomes from each parent combine.
Chromosomes carry the units of inheritance
called genes.
Chromosomes And Genes
Genes consist of DNA and contain instructions for
protein synthesis.
Chromosomes are studied to understand the nature and
working of genes.
Body cells have a constant number of paired
chromosomes, with 23 pairs in humans.
Homologous chromosomes separate during meiosis and
enter into gametes.
Chromosomes are made of chromatin material, which is
a complex material made of DNA and proteins.
DNA wraps around histone proteins to form
nucleosomes, which look like "beads on a string."
Nucleosomes and DNA between them condense into
compact forms to create chromosomes
Chemical composition of chromosome
The Watson and Crick model of DNA
How Does the DNA of
Chromosome work?
DNA is the genetic material that contains
instructions to direct all cell functions.
DNA gives instructions for the synthesis of
specific proteins.
Proteins perform structural roles and act as
enzymes to control biochemical reactions of
cells.
DNA controls all cell functions, making it
responsible for the traits and characteristics
of cells and organisms.
1. Traits are determined by specific proteins,
which have a specific number and sequence
of amino acids.
2. DNA controls the sequence of amino acids
through the sequence of its nucleotides.
3. During protein synthesis, the sequence of
DNA nucleotides is transcribed into mRNA
nucleotides in a process called transcription.
4. mRNA carries the nucleotide sequence to the
ribosome.
5. The ribosome reads the mRNA sequence and
joins specific amino acids together to form a
protein in a process called translation.
Working of DNA (also called the Central
Dogma)
Gene & Loci
A gene is a part of DNA that contains
instructions for the synthesis of a particular
protein.
Each chromosome contains thousands of
genes.
Genes occur in pairs, with one gene located
on each homologous chromosome.
The locations or positions of genes on
chromosomes are known as loci (singular:
locus).
Location of alleles on
chromosomes
Genes & Allels
Each gene determines a specific trait in an organism
Each individual carries at least one pair of genes for
each trait
Pairs of genes are represented by letters or symbols
Both members of a gene pair may be the same (AA,
aa, BB) or different (Aa, Bb)
Different forms of a gene are called alleles
Alleles are located on homologous chromosomes
Alleles separate during meiosis and each gamete
receives one allele
Offspring receive one allele from each parent
Genotype and its Types
Genotype refers to the specific combination of genes
in an individual
There are two types of genotypes: homozygous and
heterozygous
Homozygous genotype has two identical alleles (AA
or aa)
Heterozygous genotype has two different alleles (Aa)
For the trait of albinism, represented by alleles 'A' and
'a', three genotypes are possible: AA, Aa, and aa
Homozygous genotype masks or prevents the
expression of the other allele
Heterozygous genotype has one dominant allele and
one recessive allele
Dominant alleles & Recessive alleles
 Dominant alleles are represented by capital letters, while
recessive alleles are represented by lowercase letters
 Albinism is a recessive trait, expressed when both alleles
are recessive (aa)
 In humans, allele 'A' produces normal body pigments,
while allele 'a' does not produce pigments
 Genotypes AA or Aa produce pigments, while genotype aa
does not produce pigments, resulting in albinism
 Allele 'A' dominates over 'a', suppressing its effect in the
Aa genotype
 The expression of genotype as a physical trait is known as
the phenotype
 A dominant allele only suppresses the expression of a
recessive allele, it does not change its nature

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