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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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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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
(Ebook) Conservation and the genomics of populations by Margaret Byrne; Sally N. Aitken; Gordon Luikart; Frederick William Allendorf; W. Chris Funk ISBN 9780198856566, 9780198856573, 0198856563, 0198856571 All Chapters Instant Download