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![Page 1: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/1.jpg)
Bridget, Jephte, Kristi, Matt, Teresa1. Set up 20 µl mix for each primer/DNA combo (ie ex/ex
and in/in) on ice!1. 2 µl 10x F primer (1 pMol/µl = 1µM final [])2. 2 µl 10x R primer3. 1 µl DNA : use phusion amplicon for the internals if
available, if not, use genomic DNA2. We will prepare Phusion master mix for 340 µl total
volume1. 68 µl 5x Phusion HF buffer2. 6.8 µl 10 mM dNTP (200 µM final [])3. 166.4 µl water4. 3.4 µl Phusion polymerase
3. Add 15 µl master mix to each rxn4. run on touchdown starting at 72˚ C annealing T
![Page 2: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/2.jpg)
Sequencing technologies Gene Regulation•Ion Torrent Trancriptional repressors•Illumina Circular RNA•Pyrosequencing (454) Long non-coding RNA•Solid RNA transcriptional activators•Pacific Bio miRNA•Nanopore Pol II pausing
Pol IV and Pol VChromatin remodeling
Digital (Droplet) PCR RNA localizationRNA degradationRNA terminationProtein degradationMetabolomicsMito/Cp gene regulation
http://www.biotechniques.com/news/
![Page 3: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/3.jpg)
How to make a cell?Must put all the right pieces in all the right places
![Page 4: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/4.jpg)
How to make a cell?Must put all the right pieces in all the right placesSome mt & cp proteins contain subunits encoded by organelle’s genome
![Page 5: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/5.jpg)
Plastid DNAcoordination with nucleusCP signals to nucleus: retrograde signaling•ROS•Redox•Mg-protoporphyrin•Genome-uncoupled (gun) mutants are defective in retrogradesignaling
![Page 6: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/6.jpg)
Mito DNA range from 6 kb in Plasmodium to 2500 kb (muskmelons)
![Page 7: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/7.jpg)
Mito DNA range from 6 kb in Plasmodium to 2500 kb (muskmelons)•7 fold variation in mt genome size within cucurbit family•watermelon =330 kb, muskmelon = 2500 kb•considerable variation within same species•5 different cytotopes in maize, vary from 540-700kb
![Page 8: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/8.jpg)
Mito DNA range from 6 kb in Plasmodium to 2500 kb (muskmelons)• reason for large size is unknown• human mtDNA encodes 13 proteins, also rRNA & tRNA
• subunits of ATP synthase, NADHdeH, CytBC1 & COX
![Page 9: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/9.jpg)
Mito DNA human mtDNA encodes 13 proteins, also rRNA & tRNAdefects in mt DNA are nasty!
•LHON (Leber's Hereditary Optic Neuropathy is due to defects in mt-encoded subunits of NADH-deH
•ND1, ND4 or ND6mutations all havesame effect = loss of vision, sometimes MS-like symptoms
![Page 10: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/10.jpg)
Mito DNA defects in mt DNA are nasty!
•LHON •MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes)•ND1, ND5, TH, TL1& TV genes can cause it• TH,TL1 & TV encodetRNA!
![Page 11: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/11.jpg)
Mito DNA defects in mt DNA are nasty!
•LHON •MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes)•Others: cyclic vomitingsyndrome, cox deficiency, Deafness, ragged red fiber,Exercise intolerance
![Page 12: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/12.jpg)
Mito DNA defects in mt DNA are nasty!
•All show maternal inheritance (used to trace human ancestry)
![Page 13: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/13.jpg)
Mito DNA defects in mt DNA are nasty!
•All show maternal inheritance•Penetrance varies depending upon proportion of defective mt
![Page 14: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/14.jpg)
Mito DNA defects in mt DNA are nasty!
•All show maternal inheritance•Penetrance varies depending upon proportion of defective mt: average ~ 5 DNA/mt, 100 mt/cell
![Page 15: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/15.jpg)
Mito DNA defects in mt DNA are nasty!
•All show maternal inheritance•Penetrance varies depending upon proportion of defective mt•Mutations increase with age! Mutate 10x faster than nDNA due to ROS
![Page 16: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/16.jpg)
Mito DNA Mutations increase with age! Mutate 10x faster than nDNA•Defects are associated with cancer & other diseases
![Page 17: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/17.jpg)
Mito DNA defects in mt DNA are nasty!
•Mutations increase with age•Defects are associated with cancer & other diseases
![Page 18: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/18.jpg)
Mito DNA Oddities•Vertebrates, inverts, protists and & fungi have UGA = trp cf stop • In verts AUA = met cf isoleu• All sorts of other oddities in various
groups
![Page 19: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/19.jpg)
Mito DNA Human Oddities•28 genes on “heavy” strand
![Page 20: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/20.jpg)
Mito DNA Human Oddities•28 genes on “heavy” strand•9 on “light” strand, ND6 & 8 tRNAs
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Mito DNA Human Oddities•3 promoters: 2 on H strand, one on L• pL transcribes entire light strand; later
processed into tRNA & ND6
![Page 22: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/22.jpg)
Mito DNA Human Oddities•3 promoters: 2 on H strand, one on L• pL transcribes entire light strand; later
processed into tRNA & ND6• pH1 transcribes entire H strand
![Page 23: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/23.jpg)
Mito DNA Human Oddities•3 promoters: 2 on H strand, one on L• pL transcribes entire light strand; later
processed into tRNA & ND6• pH1 transcribes entire H strand• pH2 may transcribe12S & 16S rRNA
![Page 24: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/24.jpg)
Mito DNA Human Oddities•3 promoters: 2 on H strand, one on L• pL transcribes entire light strand; later
processed into tRNA & ND6• pH1 transcribes entire H strand• pH2 may transcribe12S & 16S rRNA
•In vitro only need TFAM & TFB2M to transcribe pL & pH1
![Page 25: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/25.jpg)
Mito DNA Human Oddities•3 promoters: 2 on H strand, one on L• pL transcribes entire light strand; later
processed into tRNA & ND6• pH1 transcribes entire H strand• pH2 may transcribe12S & 16S rRNA
•In vitro only need TFAM & TFB2M to transcribe pL & pH1•Uncertain if pH2 is used
![Page 26: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/26.jpg)
Mito DNA Human Oddities•DNA replication: controlled by nuclear genes
![Page 27: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/27.jpg)
Mito DNA Human Oddities•DNA replication: controlled by nuclear genes•Separate origins for H and L strands!
![Page 28: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/28.jpg)
DNA replication: controlled by nuclear genes•Separate origins for H and L strands! •Replicates in D-loop manner: starts at OH & heads towards OL displacing opposite strand until hits OL & new fork starts replicating in opposite direction.
![Page 29: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/29.jpg)
Mito DNA range from 6 kb in Plasmodium to 2500 kb (muskmelons)•7 fold variation in mt genome size within cucurbit family•watermelon =330 kb, muskmelon = 2500 kb•considerable variation within same species•5 different cytotopes in maize, vary from 540-700kb
![Page 30: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/30.jpg)
Plant Mito DNA encodes ~13 proteins, also rRNA & tRNA
• subunits of ATP synthase & complexes I, II, III & IV• some mRNA are trans-spliced from 2 diff transcripts!
![Page 31: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/31.jpg)
Mito DNA encodes encodes ~13 proteins, also rRNA & tRNA
• subunits of ATP synthase & complexes I, II, III & IV• some mRNA are trans-spliced from 2 diff transcripts!• some mRNA are edited: bases changed after synthesis!
![Page 32: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/32.jpg)
Mito DNA encodes encodes ~13 proteins, also rRNA & tRNA
• subunits of ATP synthase & complexes I, II, III & IV• some mRNA are trans-spliced from 2 diff transcripts!• some mRNA are edited: bases changed after synthesis!•Mech to prevent nucleus from stealing genes?
•Find cp & nuc genes in mtDNA!
![Page 33: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/33.jpg)
Mitochondrial DNA• some mRNA are trans-spliced from 2 diff transcripts!• some mRNA are edited: bases changed after synthesis!•Mech to prevent nucleus from stealing genes?• mtDNA recombines to form new genes: see many smaller molecules cf one big circle
![Page 34: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/34.jpg)
Mitochondrial DNA•mtDNA recombines to form new genes: see many smaller molecules cf one big circle: some poison pollen development to create cytoplasmic male sterility
![Page 35: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/35.jpg)
Mitochondrial DNA• mtDNA recombines to form new genes, some poison pollen development to create cytoplasmic male sterility•Pollen don't transmit mito!
![Page 36: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/36.jpg)
Mitochondrial DNA• mtDNA recombines to form new genes, some poison pollen development to create cytoplasmic male sterility•Pollen don't transmit mito!•May be due to PCD (apoptosis)
![Page 37: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/37.jpg)
Mitochondrial DNA• mtDNA recombines to form new genes, some poison pollen development to create cytoplasmic male sterility•Pollen don't transmit mito!•May be due to PCD (apoptosis)•Only have seenendoG in plant mt
![Page 38: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/38.jpg)
Mitochondrial DNA• mtDNA recombines to form new genes, some poison pollen development to create cytoplasmic male sterility•Pollen don't transmit mito!•Widely used in plant breeding
•Eg hybrid corn
![Page 39: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/39.jpg)
CMS• mtDNA recombines to form new genes, some poison pollen development to create cytoplasmic male sterility•described in over 150 different spp.can affect either sporophytic or gametophytic tissueeither pollen or tapetum can blow up
![Page 40: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/40.jpg)
CMSeither pollen or tapetum can blow uphave major increase in respiration and # mt after meiosis40 x increase in mt/ cell in tapetum20x in sporogenous cells
![Page 41: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/41.jpg)
CMScan (usually) be overcome by nuclear "restorer" genes usually a single dominant gene
![Page 42: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/42.jpg)
CMScan (usually) be overcome by nuclear "restorer" genes usually a single dominant gene mtDNA recombines to form new defective proteins, Nucleus fixes them
![Page 43: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/43.jpg)
Apoptosis (programmed cell death)Occurs as normal part of developmentIs also triggered by many kinds of damage
Especially to DNA
![Page 44: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/44.jpg)
Cell death vs necrosis Necrosis:Necrosis:
– Passive
– Indiscriminate
– Often follows irreversible injury
– Characterized by progressive loss of membrane integrity swelling of cytoplasm, release of cell constituents
PCDPCD– Active – Orderly process
mediated by intracellular death programs
– May or may not be due to an external factor
– Nuclear condensation
– Condensation of PM
![Page 45: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/45.jpg)
Programmed cell death (PCD)
Dev’l cell Dev’l cell deathdeath– Cell plays
active role in its demise
– Genetically controlled
Pathways
– Apoptosis
– Autophagy
– Plant PCD
(Scott & Logan, 2008, Plant Signaling & Behavior)
![Page 46: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/46.jpg)
PCD
Mammalian apoptosisMammalian apoptosis– e.g. patterning of hands/feet
PhasesPhases– Induction (perception)
– Effector (commitment)
– Degradation (dismantling of cell contents)
syndactyly
![Page 47: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/47.jpg)
http://bifi.unizar.es/research/pro_pro_inter_elec_transfer/research.php
Mitochondria --Mitochondria --sensor of death signals &sensor of death signals &initiator of biochem initiator of biochem processes leading to cell processes leading to cell deathdeath
PCD : role of mitochondrion
![Page 48: Bridget, Jephte, Kristi, Matt, Teresa 1.Set up 20 µl mix for each primer/DNA combo (ie ex/ex and in/in) on ice! 1.2 µl 10x F primer (1 pMol/µl = 1µM final.](https://reader035.fdocuments.in/reader035/viewer/2022062518/56649d0c5503460f949e0489/html5/thumbnails/48.jpg)
Programmed cell death (PCD)– Autophagy• Intracellular recycling process – lysosomes
(animals);vacuoles (plants) -- hydrolases
• Can be used to prevent premature cell death
• Upregulated PCD
(Scott & Logan, 2008, Plant Signaling & Behavior)
Apoptosis
Autophagy
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Programmed cell death (PCD)– Plant PCD• Changes in shape and position of mitochondria
(Mitochondrial morphology transition, MMT)
• Nuclear condensation
• Condensation of PM from cell wall
• Deregulated: dev’l defects, lethality
(Scott & Logan, 2008, Plant Signaling & Behavior)
MMT
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Apoptosis (programmed cell death)Occurs as normal part of developmentIs also triggered by many kinds of damage
Especially to DNAMany cancer cells do not commit apoptosis
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Apoptosis (programmed cell death)Occurs as normal part of developmentOrdered process that breaks cell into easily recycledpieces
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Apoptosis (programmed cell death)Occurs as normal part of developmentOrdered process that breaks cell into easily recycledpieces Caspases digest proteins
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Apoptosis (programmed cell death)Ordered process that breaks cell into easily recycledpieces Caspases digest proteinsCAD digests DNA
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Apoptosis (programmed cell death)Occurs as normal part of developmentTwo basic steps: commitment and execution
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Apoptosis (programmed cell death)Occurs as normal part of developmentTwo basic steps: commitment and executionCommitment depends on interplay between various signalsBax & Bcl2 have opposite effects
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Apoptosis (programmed cell death)Two basic steps: commitment and executionCommitment depends on interplay between various signalsBax & Bcl2 have opposite effects2 main pathways: extrinsic & intrinsic
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Apoptosis (programmed cell death)2 main pathways: extrinsic & intrinsicTumor necrosis factor and Fas ligand = extrinsic signals that can trigger apoptosis
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Apoptosis (programmed cell death)2 main pathways: extrinsic & intrinsicTumor necrosis factor and Fas ligand = extrinsic signals that can trigger apoptosisBind receptors in PM (TNFR or fas)
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Tumor necrosis factor and Fas ligand = extrinsic signals that can trigger apoptosisBind receptors in PM (TNFR or fas)Receptors activate FADD & TRADD: Adaptors with death domains that bind receptor’s DDs
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Receptors activate FADD & TRADD: Adaptors with death domains that bind receptor’s DDsProcaspase 8 binds FADD
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Receptors activate FADD & TRADD: Adaptors with death domains that bind receptor’s DDsProcaspase 8 binds FADD Procaspase 8 is processed to caspase 8= initiator caspase
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Procaspase 8 binds FADD Procaspase 8 is processed to caspase 8= initiator caspaseCaspase 8 converts procaspase 3 to active form = executioner
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Procaspase 8 binds FADD Procaspase 8 is processed to caspase 8= initiator caspaseCaspase 8 converts procaspase 3 to active form = executionerCaspase-3 & CAD execute the cell
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Intrinsic pathwayUsually Bcl-2 protects mitoIntracellular damage activates Bad or Bax
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ApoptosisUsually Bcl-2 protects mitoIntracellular damage activates Bad or BaxBad/Bax releases cyt c & AIF
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ApoptosisIntracellular damage activates Bad/BaxBad/Bax release cyt c & AIFCyt c, Apaf-1 & procaspase-9 form complex = apoptosome
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ApoptosisIntracellular damage activates Bad/BaxBad/Bax release cyt c & AIFCyt c, Apaf-1 & procaspase-9 form complex = apoptosomeApoptosome processes procaspase -9 to caspase-9 = initiator caspase
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ApoptosisIntracellular damage activates Bad/BaxBad/Bax release cyt c & AIFCyt c, Apaf-1 & procaspase-9 form complex = apoptosomeApoptosome processes procaspase -9 to caspase-9 = initiator caspaseCaspase-9 converts caspase 3 to active form = executioner
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ApoptosisIntracellular damage activates Bad/BaxBad/Bax release cyt c & AIFCyt c, Apaf-1 & procaspase-9 form complex = apoptosomeApoptosome processes procaspase -9 to caspase-9 = initiator caspaseCaspase-9 converts caspase 3 to active form = executionerCaspase 3 & CADexecute the cell
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ApoptosisIntracellular damage activates Bad/BaxBad/Bax release cyt c & AIFAIF induces CAD
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ApoptosisIntracellular damage activates Bad/BaxBad/Bax release cyt c & AIFAIF induces CADDestroys DNA
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ApoptosisIntracellular damage activates Bad/BaxBad/Bax release cyt c & AIFAIF induces CADDestroys DNAFlips PS outsidePhagocytic cells eatvesicles with external PS
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ApoptosisTwo basic steps: commitment and executionCommitment depends on interplay between various signalsTNF often stimulates recovery instead!