DNA carries genetic information from parents to offspring. It contains instructions for protein synthesis. DNA is a double-stranded complex made of deoxyribose, phosphate groups, and four nitrogen bases. Watson and Crick discovered the DNA double helix structure. Genetic disorders can be caused by missing or defective genes, or chromosomal abnormalities. There are four main types of genetic disorders: chromosomal disorders caused by structural or numerical chromosomal abnormalities, mutations in a single gene, multifactorial inheritance from multiple genes and environmental factors, and mitochondrial disorders in mitochondrial DNA.
DNA carries genetic information from parents to offspring. It contains instructions for protein synthesis. DNA is a double-stranded complex made of deoxyribose, phosphate groups, and four nitrogen bases. Watson and Crick discovered the DNA double helix structure. Genetic disorders can be caused by missing or defective genes, or chromosomal abnormalities. There are four main types of genetic disorders: chromosomal disorders caused by structural or numerical chromosomal abnormalities, mutations in a single gene, multifactorial inheritance from multiple genes and environmental factors, and mitochondrial disorders in mitochondrial DNA.
DNA carries genetic information from parents to offspring. It contains instructions for protein synthesis. DNA is a double-stranded complex made of deoxyribose, phosphate groups, and four nitrogen bases. Watson and Crick discovered the DNA double helix structure. Genetic disorders can be caused by missing or defective genes, or chromosomal abnormalities. There are four main types of genetic disorders: chromosomal disorders caused by structural or numerical chromosomal abnormalities, mutations in a single gene, multifactorial inheritance from multiple genes and environmental factors, and mitochondrial disorders in mitochondrial DNA.
• DNA CARRIES GENETIC INFORMATION TO OFFSPRING OF AN ORGANISM.
• IT CONTAIN HEREDITARY INFORMATION.
• IT CONTAIN INSTRUCTION FOR THE SYNTHESIS OF PROTEIN IN RIBOSOMES.
DNA→RNA→PROTEIN (CENTRAL DOGMA)
• MITOCHONDRIAL DNA IS CALLED NO CHROMOSOMAL DNA.
STRUCTURE OF DNA • CELL → NUCLEUS → CHROMATIN → CHROMOSOME → DNA → GENE • WATSON AND CRICK FIRST DISCOVERED THE DOUBLE HELIX MODEL OF DNA • DNA IS MADE UP OF FOLLOWING COMPONENTS. 1. SUGAR (DEOXYRIBOSE) 2. PHOSPHATE GROUP 3. NITROGEN BASE • PURINE (ADENINE & GUANINE). • PIRIMIDINE (THYMINE & CYTOSINE). • DNA IS A DOUBLE-STRANDED COMPLEX NUCLEIC ACID. • IT IS FORMED BY DEOXYRIBOSE, PHOSPHORIC ACID AND FOUR TYPES OF BASES. • EACH DNA MOLECULE CONSISTS OF TWO POLYNUCLEOTIDE CHAINS, WHICH ARE TWISTED AROUND ONE ANOTHER IN THE FORM OF A DOUBLE HELIX. • THE TWO CHAINS ARE FORMED BY THE SUGAR DEOXYRIBOSE AND PHOSPHATE WHICH FORM THE BACKBONE OF DNA MOLECULE. • STRANDS OF DNA ARE ARRANGED IN SUCH A WAY THAT BOTH ARE BOUND BY SPECIFIC PAIRS OF BASES. • THE ADENINE OF ONE STRAND BINDS SPECIFICALLY WITH THYMINE OF OPPOSITE STRAND. SIMILARLY, CYTOSINE OF ONE STRAND BINDS WITH GUANINE OF OTHER STRAND. • DNA FORMS COMPONENT OF CHROMOSOMES, WHICH CARRIES THE HEREDITARY INFORMATION. HEREDITARY INFORMATION THAT IS ENCODED IN DNA IS CALLED GENOME. • DNA IS A POLYNUCLEOTIDE CHAIN WHICH CONTAIN PHOSPHATE GROUP, NITROGEN BASE AND DEOXYRIBOSE SUGAR. • SUGAR + PHOSPHATE + N2 BASE → NUCLEOTIDE • SUGAR + PHOSPHATE → NUCLEOSIDE • ANY KIND OF INDIVIDUAL HAS UNIQUE DNA LIKE FINGER PRINTS. • ONLY IDENTICAL TWINS HAVE SAME DNA. • DNA HAVE LOW MUTATION TENDENCY THAT’S WHY IT IS MOST STABLE FORM OF GENETIC MATERIAL. GENE • GENE IS THE BASIC HEREDITARY UNIT OF CELL. IT IS A PORTION OF DNA CH MOLECULE THAT CONTAINS THE MESSAGE OR CODE FOR SYNTHESIS AB OF A SPECIFIC PROTEIN FROM AMINO ACIDS • THERE ARE 20 AMINO ACIDS AND THERE IS SEPARATE CODE FOR EACH AMINO ACID. • IN NUCLEOTIDE OF DNA, THREE OF SUCCESSIVE BASE PAIRS ARE TOGETHER CALLED A TRIPLET OR A CODON. EACH CODON CODES OR FORMS CODE WORD (INFORMATION) FOR ONE AMINO ACID. • THE TRIPLET CCA IS THE CODE FOR GLYCINE AND GGC IS THE CODE FOR PROLINE. GENETIC DISORDERS • GENETIC DISORDERS IS A DISEASE CONDITION THAT MAY BE OCCURS DUE TO... 1. ABSENCE OF GENE 2. DEFECTIVE GENE 3. CHROMOSOMAL ABNORMALITIES • CAUSES OF GENETIC DISORDERS. • 1. GENETIC VARIATION: PRESENCE OF A GENE THAT DIFFERS FROM NORMAL GENE. • 2. GENETIC MUTATION: ALTERATION OR A CHANGE IN NATURE, FORM, OR QUALITY. GENETIC MUTATION REFERS TO CHANGE OF THE DNA SEQUENCE WITHIN A GENE OR CHROMOSOME OF AN ORGANISM, WHICH RESULTS IN THE CREATION OF A NEW MOCHARACTER. CLASSIFICATION OF GENETIC DISORDERS • THERE ARE FOUR TYPES OF GENETIC DISORDERS... CHROMOSOMAL DISORDERS • CAUSED BY ABNORMALITIES IN CHROMOSOME. • CHANGE MAY BE HAPPEN IN STRUCTURAL & NUMBERS. 1. I. STRUCTURAL ABNORMALITY→ (ALTERATION) OF CHROMOSOMESWHICH LEADS TO DISORDERS LIKE CHROMOSOME INSTABILITYSYNDROMES 2. NUMERICAL ABNORMALITY →…… (A) MONOSOMY → DUE TO ABSENCE OF ONE CHROMOSOME FROM NORMAL DIPLOID NUMBER. EXAMPLE IS TURNER SYNDROME B. TRISOMY→ DUE TO THE PRESENCE OF ONE EXTRA CHROMO- SOME ALONG WITH NORMAL PAIR OF CHROMOSOMES IN THE CELLS. THANK YOU DR. KAVITA MEENA♥️