Structure and Function of DNA



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Structure and Function of DNA DNA and RNA Structure DNA and RNA are nucleic acids. They consist of chemical units called nucleotides. The nucleotides are joined by a sugar-phosphate backbone. The four nucleotides found in DNA differ in their nitrogenous bases. These bases are: Thymine (T) Cytosine (C) Adenine (A) Guanine (G) RNA has uracil (U) in place of thymine. Watson and Crick s Discovery of the Double Helix James Watson and Francis Crick determined that DNA is a double helix. Watson and Crick used X-ray crystallography data to reveal the basic shape of DNA. Rosalind Franklin collected the X-ray crystallography data. The model of DNA is like a rope ladder twisted into a spiral. The ropes at the sides represent the sugar-phosphate backbones. Each wooden rung represents a pair of bases connected by hydrogen bonds. DNA bases pair in a complementary fashion: Adenine (A) pairs with thymine (T) Cytosine (C) pairs with guanine (G) DNA Replication When a cell reproduces, a complete copy of the DNA must pass from one generation to the next. Watson and Crick s model for DNA suggested that DNA replicates by a template mechanism. DNA can be damaged by ultraviolet light. DNA polymerases: Are enzymes Make the covalent bonds between the nucleotides of a new DNA strand Are involved in repairing damaged DNA DNA replication in eukaryotes: Begins at specific sites on a double helix Proceeds in both directions How an Organism s Genotype Determines Its Phenotype An organism s genotype is its genetic makeup, the sequence of nucleotide bases in DNA. The phenotype is the organism s physical traits, which arise from the actions of a wide variety of proteins. DNA specifies the synthesis of proteins in two stages: Transcription, the transfer of genetic information from DNA into an RNA molecule Translation, the transfer of information from RNA into a protein

The function of a gene is to dictate the production of a polypeptide. A protein may consist of two or more different polypeptides From Nucleotides to Amino Acids: An Overview Genetic information in DNA is: Transcribed into RNA, then Translated into polypeptides What is the language of nucleic acids? In DNA, it is the linear sequence of nucleotide bases. A typical gene consists of thousands of nucleotides. A single DNA molecule may contain thousands of genes. When DNA is transcribed, the result is an RNA molecule. RNA is then translated into a sequence of amino acids in a polypeptide. What are the rules for translating the RNA message into a polypeptide? A codon is a triplet of bases, which codes for one amino acid. The Genetic Code The genetic code is: The set of rules relating nucleotide sequence to amino acid sequence Shared by all organisms Of the 64 triplets: 61 code for amino acids 3 are stop codons, indicating the end of a polypeptide Transcription: From DNA to RNA Transcription: Makes RNA from a DNA template Uses a process that resembles DNA replication Substitutes uracil (U) for thymine (T) RNA nucleotides are linked by RNA polymerase. Initiation of Transcription The start transcribing signal is a nucleotide sequence called a promoter. The first phase of transcription is initiation, in which: RNA polymerase attaches to the promoter RNA synthesis begins RNA Elongation During the second phase of transcription, called elongation: The RNA grows longer The RNA strand peels away from the DNA template Termination of Transcription During the third phase of transcription, called termination:

RNA polymerase reaches a sequence of DNA bases called a terminator Polymerase detaches from the RNA The DNA strands rejoin The Processing of Eukaryotic RNA After transcription: Eukaryotic cells process RNA Prokaryotic cells do not RNA processing includes: Adding a cap and tail Removing introns Splicing exons together to form messenger RNA (mrna) Translation: The Players Translation is the conversion from the nucleic acid language to the protein language Messenger RNA (mrna) Translation requires: mrna ATP Enzymes Ribosomes Transfer RNA (trna) Transfer RNA (trna) Transfer RNA (trna): Acts as a molecular interpreter Carries amino acids Matches amino acids with codons in mrna using anticodons Ribosomes Ribosomes are organelles that: Coordinate the functions of mrna and trna Are made of two protein subunits Contain ribosomal RNA (rrna) A fully assembled ribosome holds trna and mrna for use in translation. Translation: The Process Translation is divided into three phases: Initiation Elongation Termination Initiation

Initiation brings together: mrna The first amino acid, Met, with its attached trna Two subunits of the ribosome The mrna molecule has a cap and tail that help it bind to the ribosome. Initiation occurs in two steps: First, an mrna molecule binds to a small ribosomal subunit, then an initiator trna binds to the start codon. Second, a large ribosomal subunit binds, creating a functional ribosome. Elongation Elongation occurs in three steps. Step 1, codon recognition: the anticodon of an incoming trna pairs with the mrna codon at the A site of the ribosome. Step 2, peptide bond formation: The polypeptide leaves the trna in the P site and attaches to the amino acid on the trna in the A site The ribosome catalyzes the bond formation between the two amino acids Step 3, translocation: The P site trna leaves the ribosome The trna carrying the polypeptide moves from the A to the P site Termination Elongation continues until: The ribosome reaches a stop codon The completed polypeptide is freed The ribosome splits into its subunits As it is made, a polypeptide: Coils and folds Assumes a three-dimensional shape, its tertiary structure Several polypeptides may come together, forming a protein with quaternary structure. Transcription and translation are how genes control: The structures The activities of cells Mutations A mutation is any change in the nucleotide sequence of DNA. Mutations can change the amino acids in a protein. Mutations can involve: Large regions of a chromosome Just a single nucleotide pair, as occurs in sickle cell anemia Types of Mutations Mutations within a gene can occur as a result of:

Base substitution, the replacement of one base by another Nucleotide deletion, the loss of a nucleotide Nucleotide insertion, the addition of a nucleotide Insertions and deletions can: Change the reading frame of the genetic message Lead to disastrous effects Mutagens Mutations may result from: Errors in DNA replication Physical or chemical agents called mutagens Although mutations are often harmful, they are the source of genetic diversity, which is necessary for evolution by natural selection. Bacteriophages Bacteriophages, or phages, are viruses that attack bacteria. Phages have two reproductive cycles. In the lytic cycle: many copies of the phage are made within the bacterial cell, and then the bacterium lyses (breaks open) In the lysogenic cycle: the phage DNA inserts into the bacterial chromosome and the bacterium reproduces normally, copying the phage at each cell division Plant Viruses Viruses that infect plants can: Stunt growth Diminish plant yields Spread throughout the entire plant Viral plant diseases: Have no cure Are best prevented by producing plants that resist viral infection Animal Viruses Viruses that infect animals are: Common causes of disease May have RNA or DNA genomes Some animal viruses steal a bit of host cell membrane as a protective envelope. The reproductive cycle of an enveloped RNA virus can be broken into seven steps. HIV, the AIDS Virus HIV is a retrovirus, an RNA virus that reproduces by means of a DNA molecule. Retroviruses use the enzyme reverse transcriptase to synthesize DNA on an RNA template. HIV steals a bit of host cell membrane as a protective envelope. The behavior of HIV nucleic acid in an infected cell can be broken into six steps. AIDS (acquired immune deficiency syndrome) is:

Caused by HIV infection and Treated with drugs that interfere with the reproduction of the virus Viroids and Prions Two classes of pathogens are smaller than viruses: Viroids are small circular RNA molecules that do not encode proteins Prions are misfolded proteins that somehow convert normal proteins to the misfolded prion version Prions are responsible for neurodegenerative diseases including: Mad cow disease Scrapie in sheep and goats Chronic wasting disease in deer and elk Creutzfeldt-Jakob disease in humans