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MICRO. 555 555 Microbial Molecular Genetics Dr.Afaf Ibrahim Shehata Botany and Microbiology Department King Saud Un

MOLECULAR GENETICS

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MICRO. 555 555 Microbial Molecular Genetics Dr.Afaf Ibrahim Shehata Botany and Microbiology Department King Saud Un

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    1. MICRO. 555 (555 Microbial Molecular Genetics) Dr.Afaf Ibrahim Shehata Botany and Microbiology Department King Saud University

    2. MOLECULAR GENETICS                                                          molecular basis of inheritance          Genes   --->   Enzymes   --->   Metabolism  (phenotype)                       Central Dogma of Molecular Biology*        DNA  -transcription-->  RNA  -translation-->  Protein                                                             Student CD Activity - 13.2 Events Protein Synthesis: INFORMATION FLOW     

    3. What is a GENE = ?    DNA is the genetic material...                                           [ but what about, retroviruses, as HIV & TMV, contain RNA ]               - a discrete piece of deoxyribonucleic acid               - linear polymer of repeating nucleotide monomers                               nucleotides* -->   A   adenine,      C   cytosine                                                            T   thymidine,   G   guanine     --> polynucleotide*

    4. Understanding Genetics     INFORMATION PROCESSING    & the    CENTRAL DOGMA        - the letters of the genetic alphabet... are the nucleotides A, T, G, & C of DNA              - the unit of information is CODON   =   genetic 'word'                                   a triplet sequence of nucleotides   'CAT'  in a polynucleotide                                   3 nucleotides  =  1 codon (word)  =  1 amino acid              - the definition of (codon) word = amino acid

    5. - Size of Human Genome: ˜ 3,000,000,000 base pairs  or 1.5b in single strand of DNA genes                                           ˜    500,000,000 possible codons (words or amino acids)              - average page your textbook  =  approx 850 words                  thus, human genome is equal to 590,000 pages   or  470 copies of bio text book                   reading at 3 bases/sec it would take you about 47.6 years  @  8h/d - 7d/w                                         WOW... extreme nanotechnology

    6. µ Mice & humans (indeed, most or all mammals including dogs, cats, rabbits, monkeys, & apes)          have roughly the same number of nucleotides in their genomes -- about 3 billion bp.                                     

    7. Experimental Proof of DNA as Genetic Material...       1.  Transformation Experiments of Fred Griffith... (1920's)              Streptococcus pneumoniae - pathogenic S strain  &  benign R                          transforming 'principle'* (converting R to S cells)  is the genetic element           2.  Oswald Avery,  Colin MacLeod,  &   Maclyn McCarty... (1940's)                         suggest the transforming substance* is DNA molecules, but...           3.  Alfred  Hershey   &   Martha  Chase's*   1952   bacteriophage experiments*...                VIRAL REPLICATION*   [ pic 1 phage infection & pic-2* & lytic/lysogenic ]                          a genetically controlled biological activity (viral reproduction)                         they did novel experiment... 1st real use radioisotopes in biology*                CONCLUSION - DNA is genetic material because                     (32P) nucleic acid not (35S) protein guides* viral replication                                                         Sumanas, Inc. animation - Life cycle of HIV virus

    8. Replication of DNA...      (Arthur Kornberg -  1959 Nobel  -  died 10/26/07)                  copying of DNA into DNA is structurally obvious???    [figure*]       Patterns of Replication* =  conservative,  semi-conservative,  &  dispersive               Matt Meselson & Frank Stahl  1958 - experimental design*                     can we separate  15N-DNA   from   14N-DNA  - (OLD DNA from NEW DNA)?                     sedimentation of DNA's  (sucrose gradients  -->  CsCl gradients*  &  picture*)              we can predict results...  figure*  &   overview &  all possible results                                                    Sumanas, Inc. animation - Meselson-Stahl DNA Replications

    9.   DNA polymerase: enzyme that copies DNA...  prokaryotic Pol I-IV  eukaryotic a & d       Pol III (pic)    req: 4-deoxy-NTP's  &  ssDNA template piece                            reads template and adds a complimentary nucleotide*                                      reads 3' to 5' and synthesizes in 5' to 3' direction...               [quicktime movie]                            proofreads*  &    bidirectional synthesis*...  &   EM pic*     Replication forks - leading  &  lagging  strands - Campbell figure*              Arthur Kornberg - 1st to synthesize DNA in test tube, died 26 Oct 2007  

    10.            Model of Replication is bacterial with DNA polymerase III...              several enzymes* form a Replication Complex (Replisome) & include:                         helicase - untwists DNA                      topoisomerase [DNA gyrase] - removes supercoils,                     single strand binding proteins - stabilize replication fork,                     Primase - makes RNA primer                     POL III - synthesizes new DNA strands                      DNA polymerase I - removes RNA primer 1 base at a time, adds DNA bases                     DNA ligase repairs Okazaki fragments (seals lagging strand 3' open holes)                                                                                             

    11.   Structure of DNA polymerase III*           copies both strands simultaneously, as DNA is Threaded Through a Replisome*           a "replication machine", which may be stationary by anchoring in nuclear matrix                 Continuous & Discontinuous replication occur simultaneously in both strands        

    12. EVENTS:      1.  DNA pol III binds at the origin of replication site in the template strand      2.  DNA is unwound by replisome complex using helicase & topoisomerase      3.  all polymerases require a preexisting DNA strand (PRIMER) to start replication,                   thus Primase adds a single short primer to the LEADING strand                   and adds many primers to the LAGGING strand      4. DNA pol III is a dimer adding new nucleotides to both strands primers                   direction of reading is 3' ---> 5' on template                   direction of synthesis of new strand is 5" ---> 3'                   rate of synthesis is substantial 400 nucleotide/sec      5. DNA pol I removes primer at 5' end replacing with DNA bases, leaves 3' hole      6. DNA ligase seals 3' holes of Okazaki fragments on lagging strand                             the sequence and       DNA Repair*

    13. Rates of DNA synthesis:         myDNAi movie of replication*                                   native polymerase: 400 bases/sec with 1 error per 109 bases                                   artificial: phophoramidite method (Marvin Caruthers, U.Colorado); ssDNA synthesis                           on polystyrene bead @ 1 base/300 sec with error rate of 1/100b      

    14. GENE Expression        the Central Dogma of Molecular Biology depicts flow of genetic information                    Transcription - copying of DNA sequence into RNA                    Translation     - copying of RNA sequence into protein                   DNA sequence ------->  RNA sequence ----->  amino acid sequence                       TAC                                   AUG                               MET             triplet sequence in DNA -->  codon in mRNA     ---->   amino acid in protein

    15. Information : triplet sequence in DNA is the genetic word [codon]         Compare Events:          Procaryotes*  vs.  Eucaryotes*  =   Separation of labor           Differences DNA vs. RNA (bases & sugars)  and its single stranded          Flow of Gene Information (FIG*) - One Gene - One enzyme (Beadle & Tatum

    16. Transcription - RNA polymerase                       RNA*polymerase  - in bacteria Sigma factor* binds promoter &  initiates*  copying*                       [pnpase]                                                    Student CD Activity 15.1 - DNA Regulatory Regions              transcription factors* are needed to recognize specific DNA sequence [motif*],                binds to promoter DNA region [ activators & transcription factors*]   *                   makes a complimentary copy* of one  of the two DNA strands  [sense strand]                  Quicktime movie of transcription*     myDNAi Roger Kornberg's movie of transcription (2006 Nobel)*

    17. Kinds of RNA  [table*]                                                        tRNA -    small,  80n,  anticodon sequence, single strand with 2ndary structure*                                    function = picks up aa & transports it to ribosome                rRNA -    3 individual pieces of RNA - make up the organelle = RIBOSOME                                  primary transcript is processed into  the 3 pieces of                                            rRNA pieces (picture*)   &    recall structure of ribosome       hnRNA -  heterogeneous nuclear RNA : large Primary Transcript RNA                                function - is the precursor of mRNA in eukaryotes                                              

    18.   hnRNA -  heterogeneous nuclear RNA : large Primary Transcript RNA                                function - is the precursor of mRNA in eukaryotes                                                 mRNA -   intermediate sizes - 100n to 400n    ( split genes*)    primary transcript & mRNA                               function - codes for amino acid sequence                were not same size?    processing (cutting) of introns & exons*    Splicesome splicing of eucaryotic genes*  [glossary]  (Sumanas, Inc. advanced animation)            structure of mRNA* -  caps & tails          role of 5' CAP and Poly-A Tails*  [glossary]          luciferase    summary of eukaryotic RNA processing*           

    19. Other classes of RNA:       small nuclear RNA  (snRNP's) - plays a structural and catalytic role in spliceosome*                     there are 5 snRNP's making a spliceosome [U1, U2, U4, U5, & U6];                     they and participate in several RNA-RNA and RNA-protein interactions    SRP (signal recognition particle) - scRNA is a component of the protein-RNA complex             that recognizes the signal sequence of polypeptides targeted to the ER - figure*    small nucleolar RNA (snoRNA)    - aids in processing of pre-rRNA transcripts for                                                             ribosome subunit formation in the nucleolus

    20. micro RNA's (micro-RNA) - also called antisense RNA & interfereing RNA;  c7-fig 19.9*                      short (20-24 nucleotide) RNAs that bind to mRNA inhibiting it.     figure*          present in MODEL eukaryotic organisms as: roundworms, fruit flies, mice, humans, &  plants (arabidopsis);        seems to help regulate gene expression by controlling the timing of developmental events via mRNA action        also inhibits translation of target mRNAs. ex:        siRNA   -->   [BARR Body*]           TRANSLATION - Making a Protein   

    21. process of making a protein in a specific amino acid sequence                                                            from a unique mRNA sequence...  [ E.M. picture* ]       polypeptides are built on the ribosome (pic) on a polysome [ animation*]       Sequence of 4 Steps in Translation...                                    [glossary]                                            1. add an amino acid to tRNA  -- >   aa-tRNA            - ACTIVATION*                                                                                                                                                                                2. assemble players [ribosome*, mRNA, aa-tRNA] - INITIATION*                 3. adding new aa's via peptidyl transferase             - ELONGATION*                        4. stopping the process                                              - TERMINATION

    22. Review the processes - initiation, elongation, & termination                                      myDNAi real-time movie of translation*     &      Quicktime movie of translation                              Review figures & parts:    Summary fig*                                            [ components,  locations,  AA-site, &  advanced animation ]                                            [ Nobel Committee static animations of Central Dogma

    23. GENETIC CODE...                ...is the sequence of nucleotides in DNA, but routinely shown as a  mRNA  code*        ...specifies sequence of amino acids to be linked into the protein               coding ratio* - # of n's...    how many nucleotides specify 1 aa                      1n = 4 singlets,  2n= 16 doublets,  3n = 64 triplets                                                                                      Student CD Activity - 11.2 - Triplet Coding              S. Ochoa  (1959 Nobel) - polynucleotide phosphorylase  can make SYNTHETIC mRNA                                                          Np-Np-Np-Np  <---->    Np-Np-Np   +   Np

    24. Marshall Nirenberg (1968 Nobel) - synthetic mRNA's                  5'-UUU-3' = phe         U + C -->  UUU,  UUC,  UCC,  CCC                                                                      UCU,  CUC,  CCU,  CUU             the Genetic CODE*  -   64 triplet codons [61 = aa   &   3 stop codons]                       universal (but some anomalies),  1 initiator codon (AUG),                        redundant but non-ambiguous, and exhibits "wobble*".

    25. GENETIC CHANGE - a change in DNA nucleotide sequence                              - 2 significant ways  mutation & recombination       

    26. 1. MUTATION -  a permanent change in an organism's DNA*that results in                                  a different codon = different amino acid sequence          Point mutation  - a single to few nucleotides change...              - deletions, insertions, frame-shift mutations*     [CAT]                                                                                  Student CD Activity - 11.2 - Triplet Coding                - single nucleotide base substitutions* :                      non-sense = change to no amino acid (a STOP codon)                                                      UCA --> UAA      ser to non                      mis-sense = different amino acid                                                       UCA --> UUA      ser to leu 

    27. Sickle Cell Anemia*  - a mis-sense mutation... (SCA-pleiotropy)                                           another point mutation blood disease - thalassemia     - Effects = no effect, detrimental (lethal), +/- functionality, beneficial     2.  Recombination (Recombinant DNA) newly combined DNA's that            [glossary]*       can change genotype via insertion of NEW (foreign) DNA molecules into recipient cell

    28. 1. fertilization* - sperm inserted into recipient egg cell --> zygote   [n + n = 2n]      2. exchange of homologous chromatids via crossing over* = new gene combo's      3. transformation*  - absorption of 'foreign' DNA by recipient cells changes cell      4. BACTERIAL CONJUGATION*   - involves DNA plasmidsg*  (F+ & R = resistance)                  conjugation may be a primitive sex-like reproduction in bacteria  [Hfr*]         5. VIRAL TRANSDUCTION  - via a viral vector ( lysogeny* &  TRANSDUCTION* )                  general transduction - pieces of bacterial DNA are                                               packaged w viral DNA during viral replication                  restricted transduction - a temperate phage goes lytic                                             carrying adjacent bacterial DNA into virus particle

    29. 6. DESIGNER GENES    -   man-made recombinant DNA molecules Designer Genes - Genetic Engineering - Biotechnology    RECOMBINANT DNA TECHNOLOGY...          a collection of experimental techniques, which allow for                    isolation, copying, & insertion of new DNA sequences into                    host-recipient cells by A NUMBER OF  laboratory protocols & methodologies

    30. Restriction Endonucleases-[glossary]*... diplotomic cuts* at unique DNA sequences,               Eco-R1-figure*                               mostly palindromes...    [Never odd or even]                    ?            5' GAATTC 3'          5' G . . . . .      +      AATTC 3'         3' CTTAAG 5'          3' CTTAA               . . . .  G 5'                          ?                                                                 campbell 7/e movie*                DNA's cut this way have sticky (complimentary) ends & can be reannealed                or spliced*  w other DNA molecules to produce new genes combos     and sealed via DNA ligase.                      myDNAi movie of restriction enzyme action

    31. Procedures of Biotechnology?    [Genome Biology Research]                 A.  Technology involved in Cloning a Gene...    [animation*  &  the tools of genetic analysis]                         making copies of gene DNA             1.  via a plasmid*   [ A.E. fig  &  human shotgun plasmid cloning  &  My DNAi movie]                2.  Librariesg...    [ library figure*  &  Sumanas animation - DNA fingerprint library ]             3.  Probesg...         [ cDNAg           &    reverse transcriptaseg                                      cDNA figure*   &            cDNA library* ]                        4.  Polymerase Chain Reactiong      &     figure 20.7*   &   animation* +  Sumanas, Inc. animation*                                                                                                                         PCR reaction protocol   &    Xeroxing DNA    &   Taq polymerase

    32. B.  Detection of a Gene...   Locating a gene (or its activity) -  Restriction Maps.            1.  Restriction mapsg...     via gel electrophoresis*   &   DNA-electropherogram*                                    2.  DNA fingerprintg...     CSI Miami - how to make one*                        a murder case* &  a rape case*  + DNA prints in Health & Society & DNA Forensic Science            3.  DNA Probe Hybridizationg...   to detect specific DNA with a probe    fig 20.5*

    33. 4.  Comparing Restriction Fragments...    to a probe                 Southerng  Blotting  fig*            Sumanas, Inc. animation - DNA electrophoresis & blotting*                     one can detect specific gene sequence in samples by binding to labeled probes

    34. 5.  DNA micro-arrays - monitor gene expression in thousands of genes & changes                     by passing cDNA of the cell's mRNA over slide with ssDNA of all cell's genes;                     DNA microchips are fabricated by high speed robotics akin to Intel chip making                     cDNA (mRNA's) are fluorescently tagged so easy to see in slide's wells.                                [microchips arrays made simultaneously by phopshoramidite method of Caruthers]           Sumanas animation - DNA chip technology*      &            myDNAi DNA microarrays

    35. 5.  Gene Sequencing - Human Genome Project                        strategy - shotgun approach* developed by Celera Genomics                                               random fragments are sequenced and then ordered                                               relative to each other via overlap & supercomputing                                     Student CD Activity - 16.1 - Sequencing Strategies                      methodology  dideoxy procedure* (development by Fred Sanger)    

    36. Surprising Size Estimates of Human Genome    &    figure*                          NHGRI researchers* have confirmed the existence of 19,599 protein-coding genes                      in the human genome and identified another 2,188 DNA segments that are                      predicted to be protein-coding genes    =   21,787 genes                               mtDNA & Y-chromosome DNA aid in search for our human ancestry    Practical Applications of DNA Technology - Some examples of What's been Do

    37. 1.  Medical... disease often involves changes in gene expression            a.  disease/infection diagnosis:                         PCR & labeled DNA probes from pathogens can help identify microbe types...                              isolate HIV RNA  --RT--> cDNA --PCR--> probe     can id... AIDS infection            b.  RFLP -  Restriction Fragment Length  Analysis - markers often inherited with disease                         what is RFLP*   genetic testing & polymorphism ---> RFLP markers to disease                      DdeI cuts Sickle gene*    (also MST II cuts Sickle Cell)

    38.                                   fragment analysis (DNA fingerprinting) also used for paternity testing                 c.  Gene Therapy... idea is to replace defective genes via  microinjection of DNA*                       requires VECTORS - fig 20.16*  (patient: ADA Deficiency & Ashanti DeSilva update)                                     SCID (severe combined immunodeficiency - a single gene enzyme defect):                                     clinical trials in 2000 resulted in 2 of 9 cured, but they developed leukemia:                                          a retroviral vector inserted a repair gene in bone marrow cells                                          near genes involved in blood cell division, thus leukemia.  trials stopped.    

    39.  2.  Pharmaceutical Products...   manufactured drugs

    40. Recombinant bacteria*  =  Humulin       &         protropin (an ethical dilemma)*                                                                                                       Student CD Activity - 17.1 - Producing Human Growth Hormone    

    41. Control of Gene Expression        How do we know a gene has been active (turned on) within cells????                                                        we look for gene's product, i.e., protein or RNA                            an increase in enzyme activity implies gene action?                             no enzyme activity suggests no gene action 

    42. but, what about pre-existing inactive enzymes converting to --> active forms                                      ZYMOGENS        - pepsinogen    ----->   pepsin                                                                  - trypsinogen   ----->   trypsin

    43. thus, we have 2 possibilities:                            1) pre-existing inactive enzyme --> active                           2) de novo (new) enzyme synthesis (gene action)

    44. Mechanism of Gene Action (turning on/off genes)  in  PROCARYOTES...         model:  LACTOSE OPERON - Jacob & Monod                  [glossary]*                                                               E. coli        (grown on)                                  glucose                           lactose             NO beta-galactosidase                                     beta-galacotsidase 

    45. OPERON* = series of mapable-linked genes controlling synthesis of protein                                     p    Rg      crp      p  O   Sg1   Sg2   Sg3        Rg (i gene)    regulator  -  makes repressor protein      what if regulator binds lactose*     p                    promoter  -  binds RNA polymerase          figure       O                   operator   -  binds repressor protein        figure         S                    structural -  make enzyme proteins          figure*                                  Sumanas, Inc. animation - Lac Operon*              Catabolic Repression

    46. Control of Gene Expression  -    in   EUKARYOTES                                                                                                             Mechanism of Gene Action (turning on/off genes) is more complex                        much more DNA     &   it's inside a compartment  (nucleus)                 and, there are no operons present                 have many more promoters - sites where RNA polymerase binds                        enhancer sequence - sites where enhancers/transcription factors bind                        transcription factors - proteins that help transcription                 but, individual genes are not contiguous, thus no operons

    47. 3 levels for eukaryotic controls*   - transcriptional,   translational,   post-translational            multiple places for control* - of whether a gene make a protein or not                                                  McGraw-Hill higher Ed movie on control of gene expression

    48. Some examples for Eukaryotic gene expression controls:                   Differential Gene Activity...   is the selective expression of genes                            i.e., different cell types express different genes [liver vs. lens cell]           1.    role of activators in selective gene expression (Differential Gene Activity*)                         ex: Steroid Hormones   (figure*)

    49. 2.   Molecular turnover -  ½ life mRNA's*   &    longevity of some proteins*          3.   Processing of RNA transcript   (figure*)                         cut/spliced in nucleus and capped for transport                                  intron - pieces cut out (non gene-proteins)                                     exons - pieces transported to cytoplasm                         alternative splicing  =   figure C17.11*    and  some examples*    ex. cont.     Eukaryotic gene expression controls:    

    50. 5.  cancer often results from gene changes affecting cell cycle control.                   cancer genes, such as adenomatous polyposis coli, which cause 15% of

    51. colorectal cancers is a tumor suppressor gene, a type of  Oncogenesg*           2 kinds of human cancer genes:           Ras (proto-oncogene) causes 30% human cancers:                    is a G-protein that promotes other cell division proteins                    a Ras mutation --> hyperactive Ras protein --> cell division   fig 19.12a

    52. p53 (tumor suppressor geneg = 50% human cancers)                    fig 19.12b*                    p53 is a transcription factor that promotes the synthesis of cell cycle                    inhibiting proteins           [DNA damage --> active p53 --> p51 gene --> protein binds to                                                                                                    cyclin dependent kinase stops cell division]                        thus a p53 mutation --> leads to excess cell division (cancer)                                  - other cancer genes can lead to new gene actions resulting in cancer                 BRCA1 and BRCA2 (tumor suppressor genes) are involved in 50% of breast cancers in humans    

    53. Organization of the Genome* -                         the structural organization of genome in eukaryotes influence its expression.            Size of Human genome:                       3million+ base pairs, or some 500,000 pages of journal Nature.                       reading a 5 bases/sec it would take you about 60 year @ 8h/d 7d/w           A definition of a GENE*.  

    54. Definition of a Gene      Mendel's Particles... unit of heredity responsible for phenotype      Morgan's Loci... he placed genes on a chromosome, i.e.,                  it's a cellular entity, that is part of chromosome & is mapable      Watson & Crick... it's a sequence of specific nucleotides along the                                            length of a double helical DNA molecule             Molecular Definition...                  length:  1 nucleotide = 0.34nm  thus tRNA = 81n x 0.34 = 27.5nm                mass:    1 nucleotide = 340amu thus tRNA = 81n x 340 = 27,540amu

    55. Modern functional definition...             a DNA sequence coding for a specific polypeptide: but, also must include...                 Split Genes...    presence of Introns & Exons :                                          eukaryotic genes contain non-coding segments (introns)                                           and coding segments (exons - that make proteins)

    56. Others DNA pieces... any definition must also include:                                          segments that code for rRNA, tRNA, & snRNP's                                          also promoters, enhancer segments, regulator genes, operators ?        BEST  ˜  "a GENE is a region of DNA that CODES for an RNA"     end.   MST II restriction cuts of normal sickle beta-gene                               ( pink is DNA sequence  &  blue = 4 gel fragments)            _________|__________________|CCTNAGG GAA _____________|____________                                                  a                  b                      c                       d

    57.    In 1978, Yuet Wai Kan and Andrees Dozy of the University of California-San Francisco showed that the restriction enzyme Mst II, which cuts normal b globin DNA at a particular site, but will not recognize and therefore will not cut DNA that contains the sickle cell mutation. Mst II recognized the sequence CCTNAGG (where N = any nucleotide). Sickle cell disease is due to a single point mutation in the beta globin gene on chromosme 11 that changes CCTGAGG to CCTGTGG. MST II restriction cuts of recessive sickle beta-gene       (blue = 3 gel fragments)            _________|___________________CCTGTGG ________________|____________                               

    58.    ¥  Sickle Cell disease occurs when the DNA sequence for glutamic acid is converted to valine. This results from a change in the nucleotide T to A. This change eliminates a site recognized by the restriction enzyme DdeI.      Restriction enzyme:   DdeI (recognition sequence:  5'-C^TNAG-3')     Southern blotting probe:   fragment of ß-globin coding sequence       Pattern result: normal cell =   3 fragments (1 large, a 201bp piece, and a 175bp piece                               sickle cell  =   2 fragments (1 large, and a 376bp piece)

    59. fig 20.9*    Thus the number of RFLP piece can indicate presence of defective alleles.    reading frame (1 codon) = CAT    point mutations at hot spots - [fig]         C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T- 1st point insertion or deletion

    60.         C-A-T-X-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A     = mutant     2nd insertion or deletion         C-A-T-X-Y-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C     = mutant 3rd insertion or deletion         C-A-T-X-Y-Z-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T-C-A-T  = norma

    61. DO  NOT  study the material below  Gene expressions in   pharmacogenomics    &   toxicogenomics  via microarrays   1 cM = about 1 Mb   TRANSPOSONS - pieces of DNA prone to moving & creating repeat sequences                  LINE - long interspersed nuclear element holds promoter & 2 genes: RT & integrase     an anomaly - RNA Recoding*

    62. Simple Tandem Repeats (short- 5n to 6n)  or trinucleotide (3n) repeats can undergo an increase in copy                      number by a process of dynamic mutation; # of tandem repeats is unique to a genetic indiv.                      Variation in the length of these repeats is polymorphic.     figure*                                    individual A has ACA repeated 65 times @ loci 121, 118, and 129                                    individual B has a different repeat pattern at these loci                      STR'sa can cause genetic diseases as well:                                       CCG trinucleotide occur in fragile sites on human chromosomes (folate-sensitive group).                                             fragile X (FRAXA) is responsible for familial mental retardation.                                             another FRAXE is responsible for a rarer mild form of mental retardation.                                             mutations of AGC repeats give rise to a number of neurological disorders

    63.  3.  Forensics - DNA fingerprinting is the vogue judicial modus operandi                       a murder case* &  a rape case*  + DNA prints in Health & Society & DNA Forensic Science                      DNA fingerprinting usually looks a 5 RFLP markers and blood is tested via                      Southern Blotting (20.10) using probes for these alleles   

    64. 4.  Environmental Clean-up...             bacteria can extract heavy metals (Cu, Pb, Ni) from the environment             & convert them into non-toxic compounds                           genetically modified bacteria may be the "miner's" of the future

    65. 5.  Franken Food...  genetically modified (GM) animals & agricultural crops         Transgenics - organisms with inserted foreign DNA in their genomes                Animals*  -  GFP novelties*  +  Dolly                                 -  animal cloning companies   --->   mammalian cloning success?                                 -  "pharm" animals (20.18*)  --->   transgenic animal movie                                      sheep carry human blood protein gene that inhibits enzymes

    66. fibrosis;                                               artificially insemination, microinjection of human gene, fertilized ova are put                                               into a surrogate sheep:                                               chimeras mated to produce homozygote- Milk tested for active protein.                Plants      - genetically modified crop plants - fig 20.19*                                 -  to get Ti plasmids in = a DNA gun*   Purdue University Gene Gun movie                                                    -  Frankenfood  &  Edible Vaccines                                                    -  National Plant Genome Initiative Plan    update  future   

    67. 6.  Synthetic Biology...   artificially manufactured biological systems                                 - virus models*                            (synthetic Biology)                                           ð  An overview of biotechnology                                                    History of Biotechnology                                                      Human Genome Project & Biotech Companies                                          HHMI  funded  DNA  Interactive  tutorial

    68. What are Introns? and What is the Role of Intron DNA? don't really know, but Percentage of non-coding DNA during evolution*  goes up.  

    69.  INTRONS - DNA Junk or sophisticated Genetic Control Elements?      Current dogma of Molecular Biology            DNA --> RNA --> Proteins,   (proteins supposedly regulate gene expression)     figure*    in 1977 Phillip Sharp & Richard Roberts discovered DNA contains introns                 intervening DNA segments that do NOT code for proteins                 a primary RNA transcript is processed by splicing to assemble protein coding exons   

    70.    Presence of Introns:  Absent in prokaryotes: they have few non-coding DNA sequences                 as eukaryotic complexity grows so does non-coding DNA    [figure]                 makes up greater than 95% of the DNA                 less than 1.5% of human genome encodes proteins, but all of DNA is transcribed                 40% of human genome is Transposons & repeat genetic elements.       Evolutionary Origins?  may have been self-splicing mobile genetic elements                                     that inserted themselves into host genomes                             Advent of Spliceosomes: catalytic RNA/protein complexes                                     that snip RNAs out of mRNAs,                             would encourage introns to proliferate, mutate, evolve

    71. that inserted themselves into host genomes                             Advent of Spliceosomes: catalytic RNA/protein complexes                                     that snip RNAs out of mRNAs,                             would encourage introns to proliferate, mutate, evolve

    72. Role of Introns?  Not Junk, but rather Genetic Control Elements          [figure*]             Micro RNAs - derived from introns? - occur in plants, animals, & fungi                          a) help control timing of developmental processes as cell proliferation,                                     apoptosis, and stem cell maintenance                          b) help tag chromatin with methyl and acetyl groups                          c) may help in alternative splicing mechanisms              

    73.    COMPLEXITY:    to build a complex structure one must have bricks & mortar,                       as well as an architectural plan.             DNA, therefore should contain both - the materials and the plan:                       a) component molecules - proteins, carbs, lipids, and nucleic acids:                                      all known living organism use the same bricks and mortar                       b) the difference between Man & Monkey is the architectural plan

    74. Where is the Architectural Information?   we've always assumed in the regulatory proteins                       Maybe it's in the non-coding mirco-RNAs (intronic elements)             Thus the greater proportion of the genome of complex organisms, the introns, isn't junk,                       but rather, it is functional RNA that regulates time dependent complexity?  

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