1 / 38

1-Regulatory RNA, 2- RNA interference and micro RNA, 3-Retroviruses,

TOPICS-I. 1-Regulatory RNA, 2- RNA interference and micro RNA, 3-Retroviruses, 4-Transposons and Retroposons, 5-Promoters and Enhancers , 6-Activating Transcription, 7-RNA Splicing and Processing, 8-Chromosomes-Nucleosomes, 9-Controlling Chromatin Remodeling and Structure.

angelica-figueroa
Télécharger la présentation

1-Regulatory RNA, 2- RNA interference and micro RNA, 3-Retroviruses,

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. TOPICS-I 1-Regulatory RNA, 2-RNA interference and micro RNA, 3-Retroviruses, 4-Transposons and Retroposons, 5-Promoters and Enhancers, 6-Activating Transcription, 7-RNA Splicing and Processing, 8-Chromosomes-Nucleosomes, 9-Controlling Chromatin Remodeling and Structure.

  2. TOPICS-II 10-Gene Regulation I, 11-Gene Regulation II, 12-Protein Synthesis

  3. Books Molecular Biology of the Cell Genes IX/X/... Any....

  4. Presentation:Topic selection/student Regulatory RNA (review and paper) RNA interference Micro RNA Transposons, Retroposons and Retroviruses Promoters and Enhancers Activating Transcription RNA Splicing and Processing Controlling Chromatin Structure and Chromatin remodeling Retroviruses Gene Regulation

  5. Evaluation: 1- Exam= 50% (Parts-I and II) 2-Presentation 1=50%* (review and specific paper, idea, concept and experimental-selected by the instructor) 2a-presentation: 40% 2b-participation: 10% (*)-Each student will make a presentation for 15 min. (for specific papers) and 20 min (for review papers) with discussion (2-3 questions).

  6. Exam (Topics plus selected papers) Open/Close book

  7. Regulatory RNA

  8. MicroRNAs Are Regulators in Many Eukaryotes • Animal and plant genomes code for many short (∼22 base) RNA molecules called microRNAs. • MicroRNAs regulate gene expression by base pairing with complementary sequences in target mRNAs. C. elegans: regulator gene lin4 and its target gene lin14 (lin: Proteins for larval development)

  9. RNA Interference Is Related to Gene Silencing • RNA interference triggers degradation of mRNAs complementary to either strand of a short dsRNA. Figure 13.21

  10. dsRNA may cause silencing of host genes. Figure 13.22

  11. What is RNA interference? Shooting down mRNA

  12. RNAi • Background • What is it? • Why use it? • The mechanism and process • Experimental considerations

  13. Plasmid Virus

  14. Jorgensen 1990 van der Krol 1990 Gene injection (pigmentation Enzyme-petunias) Expectation: more red color Co-suppression of transgene and endogenous gene. Hamilton and Baulcombe 1998 Bill Douherty and Lindbo 1993 Identification of short antisense RNA sequences dsRNA? How? Gene injection with a complete tobacco etch virus particle. Expectation: virus expression Co-suppression of transgene and virus particles via RNA. Ambros 1993 (2000) Fire and Mello 1998 Identification of small RNA in C. elegans (micro RNA) Injection of dsRNA into C. elegans RNA interference (RNAi) or silencing

  15. Shooting mRNA means RNA interference

  16. What is RNA interference? --Gene “knockdown” --A cellular mechanism that degrades unwanted RNAs in the cytoplasm but not in the nucleus. Why? --A way for the cell to defend itself.

  17. Why use RNAi? 1. The most powerful way to inhibit gene expression and acquire info about the gene’s function fast 2. Works in any cell/organism 3. Uses conserved endogenous machinery 4. Potent at low concentrations 5. Highly specific.

  18. The mechanism of small interfering RNAs (siRNAs) What happens? dsRNA is processed into shorter units (siRNAs) that guide the targeted cleavage of homologous RNA.

  19. The RNAi process RNA interference: --A type of gene regulation --Involve small RNA molecules --Induce a double stranded RNA

  20. Step 1 • dsRNA is processed into sense and antisense RNAs • 21-25 nucleotides in length • have 2-3 nt 3’ overhanging ends • Done by Dicer (an RNase III-type enzyme)

  21. The siRNAs associate with RISC (RNA- induced silencing complex) and unwind Step 2

  22. the antisense siRNAs act as guides for RISC to associate with complimentary single-stranded mRNAs. Step 3

  23. RISC cuts the mRNA approximately in the middle of the region paired with the siRNA The mRNA is degraded further Step 4

  24. ssRNA (exogenous) RNA-dependent RNA polymerase Catalysis: RdRP copies RNA making more ds RNA. Dicer complex: RNAase III with ATP hydrolysis requirement. Dicer cuts, unwinds dsRNA and generates more siRNA. More RdRP is activated and more dsRNA is made. RISC complex:RNA-Inducible Silencing Complex with ATP hydrolysis. (RdRP) (endogenous)

  25. Gene regulation by small RNAs Dicer gene in C. elegans siRNAs degrade mRNA to stop gene expression quickly Small temporal (St) RNAs prevent translation to stop gene expression quickly

  26. -your RNAi? --MicroRNAs (miRNA) are single-stranded RNA molecules of about 21-23 nucleotides in length, which regulate gene expression (down-regulation). --miRNAs are encoded by genes that are non-coding RNAs ( no proteins are made) --Stem-loop or hairpin loop intra-molecular base pairing is a pattern that can occur in single-stranded DNA or, more commonly, in RNA.

  27. Experimental Considerations • Transfection method: • 1-Lipofectamine 2000--cationic lipids to bind siRNA and neutral • lipids to allow escape from Endosomes • 2-Plamids/Viruses--express small fragment of hairpin DNA • Transfection efficiency • Negative controls --scrambled siRNA • Off-target effects: • Sense (or antisense) strand is homologous to another sequence • Activation of stress response pathways “apoptosis”

  28. http://www.nature.com/nrg/journal/v2/n2/animation/nrg0201_110a_swf_MEDIA1.htmlhttp://www.nature.com/nrg/journal/v2/n2/animation/nrg0201_110a_swf_MEDIA1.html

  29. Growth Factor Receptor Binding Protein (Grb) 2-mediated Recruitment of the RING Domain of Cbl to the Epidermal Growth Factor Receptor (EGFR) Is Essential and Sufficient to Support Receptor Endocytosis Fangtian Huang and Alexander Sorkin

  30. Knockdown of growth factor receptor binding protein 2 (Grb2) by RNA interference strongly inhibits clathrin-mediated endocytosis of the epidermal growth factor receptor (EGFR). To gain insights into the function of Grb2 in EGFR endocytosis, we have generated cell lines in which endogenous Grb2 was replaced by a modified yellow fluorescent protein (YFP)-tagged Grb2 and it was expressed at the physiological level. In these cells, Grb2-YFP fully reversed the inhibitory effect of Grb2 knockdown on EGFR endocytosis and, moreover, trafficked together with EGFR during endocytosis.

  31. To generate HeLa cells stably expressing Grb2-YFP, endogenous Grb2 was knocked down using vector-based short hairpin RNA (shRNA) with simultaneous expression of Grb2-YFP that has silencing mutations rendering this construct insensitive to shRNA.

  32. pSilencer1.0-U6 vector-- pSuper-H1 vector-- retrovirus//inducible Type III RNA pol III promoter ----U6 small nuclear promoter (U6) ----human H1 promoter (H1)

More Related