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The document describes the structure and function of DNA, highlighting its double helix formation, nucleotide composition, and role in protein synthesis. It explains the concepts of genes, chromosomes, and inheritance, detailing how traits are passed from parents to offspring and the significance of alleles in genetic variation. Additionally, it differentiates between genotype and phenotype, illustrating how genetic makeup influences observable traits.

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0% found this document useful (0 votes)
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genes & inheritance 1 new

The document describes the structure and function of DNA, highlighting its double helix formation, nucleotide composition, and role in protein synthesis. It explains the concepts of genes, chromosomes, and inheritance, detailing how traits are passed from parents to offspring and the significance of alleles in genetic variation. Additionally, it differentiates between genotype and phenotype, illustrating how genetic makeup influences observable traits.

Uploaded by

abdullahasif1956
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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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17.

2 DNA
1. Describe the structure of a DNA molecule:

(a)two strands coiled together to form a double helix


(b)each strand is made up of a chain of nucleotides
(c) each nucleotide contains a base (A, T, C, G – full names not
required)
(d)bonds between pairs of bases hold the strands together
(e)the bases always pair up in the same way: A with T, and C with
G
2 Define a gene as a length of DNA that codes for a protein
3. Explain that DNA controls cell function by controlling the
production of
proteins, including enzymes
4. State that the sequence of bases in a gene determines the
The pattern of
inheritance and variation
Heredity: tendency of an individual to
resemble his parents
Variation: the differences between
individuals of the same species
Genetics: the study of how characters /traits are
transferred or inherited from one generation
to the next & what
causes resemblance and difference among
organisms
Chromosomes -- Genetic
materials
 Genetic materials found inside the nucleus of a
cell
 Appear as very thin & thread-like structures called
Chromatins
 In dividing cell chromatin condenses to form
chromosomes
 Each specie has definite Number of
chromosomes in each cell
 Somatic cell has Diploid Number of chromosomes
i-e 2 set of chromosomes
 While gametes have half number of chromosomes
DNA-- nucleic acids – Genetic material
Chromosomes are made up of DNA and protein
• DNA controls cell function by controlling the production of proteins
DNA is very long, thin molecule-- made up of a chain of 4 different
type of nucleotides
Each nucleotide consists of ... A phosphate molecule, a pentose
sugar and one of the four nitrogen bases [A, T, C, G]
Each nucleotide is different because of different N-base
Nucleotides held by a covalent bond to make long strand of DNA
In a DNA molecule two strands coiled together to form a double helix
The strands held together by Hydrogen bonds between pairs of bases
The bases always pair up in the following way:
A double H- bonds with T and
C triple H-bond with G
gene -- Genetic materials
 Gene is unit of inheritance and is inherited to next generation
 Gene is a length of DNA along Chromosome that codes
for a protein
 The place on chromosome where gene resides is called
gene locus
 Genes specifies a particular character, responsible for synthesis of
specific protein including enzymes
• Sequence of bases in a gene determines the sequence
of amino acids needed to make a specific protein
• Different sequence of amino acids give a different
shape to protein molecule
Gene unit of inheritance
Role of chromosome in inheritance
 Chromosomes/genes inherited from one generation to
the next during reproduction
 As asexual reproduction followed by mitotic division so
chromosomes/genes are copied
 So no variation in the next generation. Resulting
progeny is exact copy of parent
 In sexual reproduction meiosis takes place during
gamete formation so homologous chromosomes
shuffled/exchange their gene
 So variation occur in the next generation. Resulting
progenies are different from parent, their hereditary
information are also not similar
Homologous Chromosomes
 In a somatic cell chromosomes exist in
matching pairs called homologous pairs
 One member of pair is inherited from mother
& other from father
 Human somatic cell has 46 chromosomes i-
e 23 pairs of homologous chromosomes
 One out of23 pairs is of sex chromosomes
while rest 22 pairs are called autosomes
 Autosomes are numbered chromosomes are
similar in shape, size and arrangement of
genes, containing genes not relating to sex
 While sex chromosomes may or may not
similar in shape, size and arrangement of
genes and contain genes relating to sex
 Genes on homologous pair also exist in form of
matching pairs
 Members of homologous chromosomes carry the
same genes, controlling same character, occur on
same loci
 Such matching pair of genes is called alleles
 Each gene specifies a trait & each trait is
controlled by two alleles
 But these alleles may be of different
forms/effects
 Alleles Alternative forms of same genes occupy the
same position in a pair of the homologous
chromosomes controlling the same character but
may have same or different expression e-g
Allele --- phenotype &
genotype
 Alleles are responsible for variation in character
 Allele exist in 2 forms --dominant & recessive
 Allele said to be dominant if always expressed in the organism and
represented by capital letter
 Allele said to be recessive if it expressed itself when it is present on
both chromosomes of pair and represented by small letter
 For a specific character Allele may be same or may be different on
both chromosomes and organism is said to be
homozygous if both alleles are same (e-g TT or tt)
heterozygous if both alleles are different (e-g Tt)
 Genotype refers to genetic makeup of an organism i-e genes & their
respective alleles
 Phenotype -- an expressed trait(that can be seen) of individual are the
result of interaction between allele’s pair, and is determined by
genotype
Genotype & Phenotype for a specific trait
 Therefore an organism may inherit one of the following
three genotypes
 Both dominant alleles 1 from each parent -homozygous
dominant (TT)
 Both recessive alleles 1 from each parent --homozygous
recessive (tt)
 1 dominant & 1 recessive alleles from each parent --
heterozygous (Tt)
 At least one of the dominant allele in genotype, then
individual show dominant feature in its phenotype.
 Thus the homozygous dominant & heterozygous
genotype will give same phenotype while homozygous
recessive have opposite phenotype.
 Homozygous are pure bred means on self fertilizing they

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