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1 . Which is the most unlikely involved in the intron-splicing of pre-mRNA ?

1 . Which is the most unlikely involved in the intron-splicing of pre-mRNA ? [ a . U1 RNP; b . 5' cap structure; c . polyadenylation signal; d . secondary structure of pre-mRNA], give a brief explanation if you are not sure your answer (5%).

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1 . Which is the most unlikely involved in the intron-splicing of pre-mRNA ?

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  1. 1.Which is the most unlikely involved in the intron-splicing of pre-mRNA ? [a. U1 RNP; b. 5' cap structure; c. polyadenylation signal; d. secondary structure of pre-mRNA], give a brief explanation if you are not sure your answer (5%)

  2. U1A protein inhibits polyadenylation of its pre-mRNA U1A protein binds U1snRNA: 7-base sequence-U1A binding site

  3. U1A protein inhibits polyadenylation of its pre-mRNA U1A binding site 2 copies in its own mRNA , at 3' end near the poly(A) signal prevent polyadenylation, but not the cleavage of pre-mRNA rapidly degraded

  4. U1A protein inhibits polyadenylation of its pre-mRNA - prevent polyadenylation, but not the cleavage of pre-mRNA truncated mRNA without poly(A) tail, rapidly degraded

  5. RNA editing in mammalian apo-B (apolipoprotein B), serum protein of lipid transporter, CAA UAA, glutamine stop codon, in intestine both liver and intestine forms transport lipid only liver apo-B delivers cholesterol containing LDL

  6. RNA editing in glutamate receptor mRNA Na+, Ca+2 ion channel, learning and memory CAG  CIG, glutamate  arginine, Ca +2 cannot pass Both editing of apo-B and glutamate receptor by RNA deaminases

  7. Iron dependent regulation of TfR mRNA stability. when iron ion high, IRE -BP inactive, cannot bind IRE, TfR mRNA is protected from degradation; when iron is low, IRE-BP is active and binds IRE. then TfR mRNA stability , TfR mRNA degraded

  8. Iron dependent regulation of translation of ferritin stability. ferritin is an intracellular protein that binds iron ions ferritin, 5' IRE free of BP, translation occurs, more ferritin. The IRE in ferritin mRNA has no AU rich

  9. ferritin

  10. Using Yeast to study Eukaryotic Gene Functionfrom Recombinant DNA (J Waston et al.) Ch 13 Size of genome in the selected organisms

  11. Yeast biosynthetic genes are cloned by complementation of E.coli mutations Cloning yeast biosynthetic genes by complementation in E.coli

  12. Shuttle vectors replicate in both E.coli and yeast Classes of yeast vectors

  13. Yeast genes can be cloned by simple complementation Cloning a yeast gene by complementation

  14. Generation of temperature sensitive mutants of yeast

  15. Replica plating

  16. Homolgous recombination is a relative frequent event in yeast Gene targeting by homologous recombination

  17. Replacing a gene by transplacement

  18. Tetrad analysis

  19. Cloning genes required for mating reveals a signaling pathway similar to that seen in higher organisms Pheromone signaling pathway

  20. This fragment DNA only works in high copies, suggesting it was acting as a suppressor Cloning of the GPA1 gene as a high-copy suppressor of pheromone sensitivity

  21. Genetic experiments in yeast can answer precise biochemical questions The receptor swap experiment

  22. U2 RNA base-pairs with an intron sequence

  23. Base pairing between U2 and branch point (in yeast)

  24. A genetic assay for protein-protein interactions

  25. Genetic analysis in yeast can be exploited to identify and study genes from higher organisms Plasmid shuffle

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