Chapter 12 DNA and RNA. DNA and RNA I. DNA- deoxyribonucleic acid A. History of DNA as Genetic Material “code of life” 1. Griffith and Transformation.

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Presentation transcript:

Chapter 12 DNA and RNA

DNA and RNA I. DNA- deoxyribonucleic acid A. History of DNA as Genetic Material “code of life” 1. Griffith and Transformation a. Frederick Griffith made discovery while investigating bacteria known to produce pneumonia b. Griffith isolated two different strains of bacteria

1). Disease causing strain- had smooth edges. When injected into mice caused pneumonia. 2). Harmless strain- grew with rough edges.

c. When disease causing bacteria heated- mice survived when injected d. Mixed the heated-killed bacteria and harmless ones. When injected caused pneumonia. Concluded that one strain had been changed into another. Called transformation.

2. Avery and DNA- group of scientists repeated Griffith’s experiment to discover “transforming” factor. a. Made extract from heat-killed bacteria b. Treated extract with enzymes that destroyed proteins, lipids, carbohydrates, and other molecules- transformation still occurred. c. Repeated using enzymes that would break down DNA. Transformation did not occur! d. Concluded- DNA carries genetic code

3. Hershey-Chase Experiment- (1952) showed conclusively that DNA was molecule that carried genetic code a. Studied viruses known as bacteriophages

b. Used different radioactive markers to label DNA and proteins of bacteriophages

B. The Structure of DNA 1. DNA made of units called nucleotides a. Nucleotides made up of 3 parts 1). 5-carbon sugar called deoxyribose 2). Phosphate group 3). Nitrogenous (nitrogen containing) base

a). Four kinds of nitrogenous bases b). Purines- include adenine and guanine b). pyrimidines- include cytosine and thymine

b. Backbone of DNA chain formed by sugar and phosphate groups of nucleotides sugar phosphate

2. Discoveries- understanding DNA’s structure a. Chargaff’s Rule- ratio of guanine:cytosine and adenine:thymine are equal A = T and G = C

b. X-Ray evidence- 1950’s Rosalind Franklin used X-ray diffraction to study structure of DNA molecule. Concluded structure was coiled like a spring (helix)

c. The Double Helix- after looking at Franklin and Wilkin’s work, Watson and Crick constructed a model of DNA molecule (1953)

1). Hydrogen bonds between base pairs holds two strands together 2). Base Pairing –explained Chargaff’s Rule A=T and C=G

Chromosomes and DNA Replication II. Chromosomes and DNA Replication A. DNA and Chromosomes- found in both eukaryotic and prokaryotic cells 1. Prokaryotic cells- DNA located in cytoplasm in single circular DNA molecule (referred to as cell’s chromosome)

2. Eukaryotic Cells- DNA located in cells nucleus in form of a number of chromosomes

B. Chromosome Structure- even the smallest of human chromosomes contains 30 million base pairs chromatin histones 1. Eukaryotic chromosomes tightly packed together to form substance called chromatin. DNA coiled around proteins called histones

Nucleosome 2. Nucleosome- DNA wrapped around histones

DNA Replication C. DNA Replication replication 1. Duplicating DNA- before cell divides, it duplicates it’s DNA in a process called replication a. DNA molecule separates into two strands b. Two new complementary strands produced (follows rules of base pairing) each strand serves as template for new strand c. Process carried out by series of enzymes (DNA polymerase)

RNA and Protein Synthesis D. RNA and Protein Synthesis 1. Structure of RNA- 3 main differences between RNA and DNA ribose a. Sugar in RNA is ribose single stranded b. RNA is single stranded uracil c. RNA contains uracil in place of thymine

Protein Synthesis 2. Most RNA involved in Protein Synthesis 3 Types of RNA 3. 3 Types of RNA Messenger RNAmRNA a. Messenger RNA (mRNA)- disposable copy of DNAto carry instructions to rest of cell Ribosomal RNArRNA b. Ribosomal RNA (rRNA)- helps to assemble proteins on ribosomes Transfer RNAtRNA c. Transfer RNA (tRNA)- transfers amino acids to ribosomes to contruct protein molecules

Transcription E. Transcription- process by which DNA makes complementary sequence of RNA 1. Enzyme (RNA Polymerase) separates DNA strand 2. One strand of DNA used as template to assemble strand of RNA. Takes place in nucleus

3. Transcription begins at specific locations on DNA (promoters)Transcription

Translations F. Translations- “making Proteins” Translating language of nucleic acids (base sequences) into language of proteins (amino acids) 1. Gene carries code to make one protein (300 to 3000 base pairs) a. Code written in language with only 4 “letters” codon b. Code read 3 letters at a time (each 3 letter “word” known as a codon UCGCACGGU UCG – CAC – GGU Represents the amino acids Serine – Histidine – Glycine

2. Process used all 3 types of RNA a. mRNA transcribed in nucleus and released into the cytoplasm AUGstart codon b. mRNA attaches to ribosome. Translation begins AUG, the start codon

anticodon codon c. Each tRNA has an anticodon whose bases are complementary to codon on mRNA. tRNA brings amino acids to ribosomes anticodon codon

d. Ribosome moves along mRNA, binding new tRNA molecules and amino acids

stop codon e. Polypeptide chain (protein) grows until ribosome reaches stop codon stop codon Protein molecule

f. Protein and mRNA released completing process of translationtranslation

Functional structural proteins G. Genes and Proteins- proteins are key to everything cells do. Functional (enzymes) and structural proteins

Mutations- III. Mutations- changes in the DNA sequence that affect genetic information Gene Mutations A. Gene Mutations- results from changes in a single gene 1. Several types- some involve several nucleotides, but most affect only one Point mutations 2. Point mutations- occurs at a single point in DNA sequence. Generally change in one of amino acids

b. Can alter protein- making it unable to perform normal functions Frameshift mutation a. Frameshift mutation- insertion or deletion of nucleotide. Causes bigger changes!

Chromosomal Mutations B. Chromosomal Mutations- involves changes in the number and structure of chromosomes

Gene Regulation C. Gene Regulation- how does organism “know” when to turn a gene on or off? repressor protein 1. Genes are “turned off” by presence of repressor protein (produced by regulator gene) repressor protein 2. Genes are “turned off” by presence of repressor protein (produced by regulator gene)

3. Presence of certain chemicals (e.g.- lactose in E. ecoli ) bind to site on repressor protein causing it to change shape and “fall off” the DNA molecule. 4. RNA plymerase is allowed to transcribe mRNA molecule to code for protein (e.g. enzymes to break apart lactose molecules)

D. Regulation and Development- especially important in shaping the way a complex organism develops from single fertilized cell. Hox genes 1. Hox genes- controls organs and tissues that develop in various parts of the embryo a. Mutation in one of these “master control genes” can completely change organs that develop in specific parts of the body b. Genes tell cells in the body which organs and structures they should develop into as the body grows. 2. Mutations may have led to drastic and quick evolutionary changes