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Central Dogma of Molecular Biology

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Presentation on theme: "Central Dogma of Molecular Biology"— Presentation transcript:

1 Central Dogma of Molecular Biology
DNA Stored information inside nucleus Copied to make new cells = REPLICATION RNA Copied from a piece of DNA (GENE) to make a single protein = TRANSCRIPTION Moves information from nucleus to cytoplasm Protein Information from a single RNA used to make a single protein = TRANSLATION

2 Base Pairing Complementary bases Complementary strands A bonds to T
C bonds to G Complementary strands Opposite strands of DNA that can completely base pair to form a double helix

3 DNA Double Helix

4 Chromatin and Chromosomes
DNA associated with proteins Organizes and packages DNA Chromosome Tightly coiled chromatin Many cells have more than one chromosome Humans – 46 chromosomes

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7 DNA Replication Each strand of DNA can act as a template for the complementary strand Enzymes guide replication

8 DNA Replication Enzymes pull apart the DNA strands
Enzymes add complementary nucleotides to each strand

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10 Transcription Part of the DNA molecule is copied to make an RNA molecule

11 The Genetic Code and Genetics
How does DNA encode for protein? DNA – nucleotide subunits Nitrogenous bases = information 4 different nitrogenous bases Protein – amino acid subunits 20 different amino acids

12 How are four nitrogenous bases translated into 20 different amino acids?
Nucleotides form “words” called codons Each codon codes for a different amino acid A codon consists of 3 nitrogenous bases 64 different combinations of codons Only 21 needed (20 amino acids, 1 stop)

13 How is the code read?

14 Transfer RNA’s “Read” codons Bring amino acids to the ribosome

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22 Mutations Changes in DNA often but not always cause changes in the protein for which it codes. Changing a single nucleotide has the potential to dramatically change a protein.

23 Gene

24 Homologous Chromosomes

25 Vocabulary Allele Homozygous Heterozygous Genotype Phenotype
Different versions of a gene Make different versions of a protein Homozygous Same allele on both homologous chromosomes Heterozygous Different allele on each homologous chromosome Often referred to as a hybrid Genotype Total set of alleles which can be passed to the next generation Phenotype Observable appearance caused by different alleles

26 Naming Genes All alleles of a gene use the same root letter or word to indicate that it is the same gene Dominant allele Phenotype expressed in heterozygous individual Capitalized letter or word = dominant gene Recessive allele Phenotype only expressed in homozygous individual Lower case letter or word = recessive gene

27 Gregor Mendel’s Law of Segregation
Alleles of a gene segregate from one generation to another Exact reason not known by Mendel Today we know assortment occurs during meiosis

28 Garden Pea Self-fertilize Cross-fertilize
Pollen from same flower Cross-fertilize Pollen from different flower To cross is to fertilize (mate)

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30 Heterozygous Cross Alleles P p Dominant Phenotype purple Recessive
Phenotype white

31 Genotype Vs. Phenotype Ratio

32 Test Cross To cross an organism with an unknown genotype with an organism with a known phenotype PP or Pp X pp Purple flower could be either PP or Pp White flower must be pp

33 Multiple Alleles

34 Incomplete Dominance

35 Linked Genes Genes close together on the same chromosome
Sort together during Meiosis Inherited together

36 Gregor Mendel’s Law of Independent Assortment
Traits are transmitted to offspring independently of one another Traits that sort independently are on different chromosomes

37 Dihybrid Cross Seed Texture Seed Color R=round r=wrinkled Y=yellow
y=green

38 Sex Chromosomes Humans 46 total chromosomes 23 pairs
22 pairs are called autosomes common to both males and females 1 pairs are called sex chromosomes Females 2 X-chromosomes Males 1 X-chromosome and 1 Y-chromosome

39 Sex Determination SRY gene present on Y-chromosome triggers male pathway Female pathway is the default Hormones determine male and female sex characteristics

40 X-Linked Traits Male inherits only one X-chromosome
From which parent? Males are Hemizygous for genes on X-chromosome Female inherits two X-chromosome One from each parent

41 Queen Victoria Pedigree

42 Dosage Compensation Both males and females require the same amount of protein coded for in their X-chromosomes However… Females 2 X-chromosome Males 1 X-chromosomes

43 X-inactivation Female embryos inactivate one X-chromosome at random in each cell when they are days old. Inactive X-chromosome is called a Barr Body Females are a mosaic

44 Calico Cats Gene for coat color on X-chromosome
Two alleles Brown and Black

45 Anhydrotic Dysplasia Sweat gland do not develop
Heterozygous females are mosaics


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