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Nucleic Acid Structure II

Nucleic Acid Structure II. Andy Howard Introductory Biochemistry 22 October 2014. DNA structure informs its functions. We will revisit several aspects of nucleic acid structure that help us understand how it operates. What we ’ l l discuss. RNA Types Functions Splicing

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Nucleic Acid Structure II

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  1. Nucleic Acid Structure II Andy HowardIntroductory Biochemistry22 October 2014 Nucleic Acid Structure II

  2. DNA structure informs its functions • We will revisit several aspects of nucleic acid structure that help us understand how it operates. Nucleic Acid Structure II

  3. What we’ll discuss • RNA • Types • Functions • Splicing • DNA tertiary structure • Nucleosomes • Higher-level structures • Bacterial organization Nucleic Acid Structure II

  4. Ribonucleic acid • We’re done with DNA for the moment. • Let’s discuss RNA. • RNA is generally, but not always, single-stranded • The regions where localized base-pairing occurs (local double-stranded regions) often are of functional significance Nucleic Acid Structure II

  5. RNA physics & chemistry • RNA molecules vary widely in size, from a few bases in length up to 10000s of bases • There are several types of RNA found in cells Type % %turn- Size, Partly Role RNA over bases DS? mRNA 3 25 50-104 no protein template tRNA 15 21 55-90 yes aa activation rRNA 80 50 102-104 yes transl. catalysis & scaffolding sRNA 2 4 15-103 yes various Nucleic Acid Structure II

  6. Messenger RNA • mRNA: transcription vehicleDNA 5’-dAdCdCdGdTdAdTdG-3’RNA 3’- U G G C A U A C-5’ • typical protein is ~500 amino acids;3 mRNA bases/aa: 1500 bases (after splicing) • Additional noncoding regions (see later) brings it up to ~4000 bases = 4000*300Da/base=1,200,000 Da • Only about 3% of cellular RNA but unstable! Nucleic Acid Structure II

  7. Relative quantities • Note that we said there wasn’t much mRNA around at any given moment • The amount synthesized is much greater because it has a much shorter lifetime than the others • Ribonucleases act more avidly on it • We need a mechanism for eliminating it because the cell wants to control concentrations of specific proteins Nucleic Acid Structure II

  8. mRNA processing in Eukaryotes Genomic DNA Unmodified mRNA produced therefrom • # bases (unmodified mRNA) = # base-pairs of DNA in the gene…because that’s how transcription works • BUT the number of bases in the unmodified mRNA > # bases in the final mRNA that actually codes for a protein • SO there needs to be a process for getting rid of the unwanted bases in the mRNA: that’s what splicing is! Nucleic Acid Structure II

  9. Splicing: quick summary Genomic DNA transcription Unmodified mRNA produced therefrom exon intron exon intron exon intron • Typically the initial eukaryotic message contains roughly twice as many bases as the final processed message • Spliceosome is the nuclear machine (snRNAs + protein) in which the introns are removed and the exons are spliced together splicing exon exon exon translation (Mature transcript) Nucleic Acid Structure II

  10. Heterogeneity via spliceosomal flexibility • Specific RNA sequences in the initial mRNA signal where to start and stop each intron, but with some flexibility • That flexibility enables a single gene to code for multiple mature RNAs and therefore multiple proteins Nucleic Acid Structure II

  11. Transfer RNA • tRNA: tool for engineering protein synthesis at the ribosome • Each type of amino acid has its own tRNA, responsible for positioning the correct aa into the growing protein • Roughly T-shaped or Y-shaped molecules; generally 55-90 bases long • 15% of cellular RNA Yeast Phe tRNA76 basesPDB 1EVV, 2Å Nucleic Acid Structure II

  12. Secondary and Tertiary Structure of tRNA • Extensive H-bonding creates four double helical domains, three capped by loops, one by a stem • Only one tRNA structure (alone) is known • Phenylalanine tRNA is "L-shaped" • Many non-canonical bases found in tRNA Nucleic Acid Structure II

  13. tRNA structure: overview Nucleic Acid Structure II

  14. Amino acid linkage to acceptor stem Amino acids are linked to the 3'-OH end of tRNA molecules by an ester bond formed between the carboxyl group of the amino acid and the 3'-OH of the terminal ribose of the tRNA. Nucleic Acid Structure II

  15. Yeast ala-tRNA • Note nonstandard bases and cloverleaf structure Nucleic Acid Structure II

  16. Ribosomal RNA • rRNA: catalyic and scaffolding functions within the ribosome • Responsible for ligation of new amino acid (carried by tRNA) onto growing protein chain • Can be large: mostly 500-3000 bases • a few are smaller (150 bases) • Very abundant: 80% of cellular RNA • Relatively slow turnover Haloarculamarismortui 23S rRNAPDB 1FFZ602 bases Nucleic Acid Structure II

  17. Small RNA • sRNA: few bases / molecule • often found in nucleus; thus it’s often called small nuclear RNA, snRNA • Involved in various functions, including processing of mRNA in the spliceosome • Some are catalytic • Typically 20-1000 bases • Not terribly plentiful: ~2 % of total RNA Protein Prp31complexed to U4 snRNAPDB 2OZB33 bases + 85kDa heterotetramerHuman Nucleic Acid Structure II

  18. Unusual bases in RNA • mRNA, sRNA mostly ACGU • rRNA, tRNA have some odd ones Nucleic Acid Structure II

  19. Other small RNAs • 21-28 nucleotides • Target RNA or DNA through complementary base-pairing • Several types, based on function: • Small interfering RNAs (q.v.) • microRNA: control developmental timing • Small nucleolar RNA: catalysts that (among other things) create the oddball bases snoRNA77courtesy Wikipedia Nucleic Acid Structure II

  20. siRNAs and gene silencing • Small interfering RNAs block specific protein production by base-pairing to complementary seqs of mRNA to form dsRNA • DS regions get degraded & removed • This is a form of gene silencing or RNA interference • RNAi also changes chromatin structure and has long-range influences on expression Viral p19 protein complexed to human 19-base siRNA PDB 1R9F1.95Å 17kDa protein Nucleic Acid Structure II

  21. Chromosome structure: levels • Each of the first 4 levels compacts DNA by a factor of 6-20; those multiply up to > 104 Nucleic Acid Structure II

  22. Nucleosome Structure • Chromatin, the nucleoprotein complex, consists of histones and nonhistone chromosomal proteins • Histone octamer structure has been solved • without DNA: Moudrianakis, 1991 • with DNA by Richmond • Nonhistone proteins are regulators of gene expression Nucleic Acid Structure II

  23. Histone types • H2a, H2b, H3, H4 make up core particle, associating with ~146 bp of DNA:two copies of each, so: protein octamer • All histones are KR-rich, small proteins • H1 associates with ~54bp region between two nucleosomes Nucleic Acid Structure II

  24. Histones: table 11.2, plus… Nucleic Acid Structure II

  25. Unfolded chromatin • Treat chromatin with low ionic strength; that disrupts higher level interactions so the individual nucleosomes are strung out relative to one another like beads on a string Image courtesy U. Maine Nucleic Acid Structure II

  26. Nucleosome core particle Nucleic Acid Structure II

  27. Half the core particle • Note that DNA isn’t really circular: it’s a series of straight sections followed by bends (like the Advanced Photon Source ring!) Nucleic Acid Structure II

  28. Histones, continued • Individual nucleosomes attach via histone H1 to seal the ends of the turns on the core and organize 40-60bp of DNA linking consecutive nucleosomes • N-terminal tails of H3 & H4 are accessible • K, S get post-translational modifications, particularly K-acetylation Nucleic Acid Structure II

  29. Histone deactivation • Histones interact with DNA via +charges on lys and arg residues. • If we neutralize those charges by acetylation, the histones don’t bind as tightly to the DNA • Carefully-timed enzymatic control of histone acetylation is a crucial element in DNA organization Nucleic Acid Structure II

  30. CoASH Histone acetylation Histone H1PDB 1GHC8.3 kDa monomerChicken • Active histone + Acetyl CoA  inactive (acetylated) histone + CoASH • Without the positive charges, the affinity for DNA goes down Histone acetyltransferasePDB 1QSO66 kDatetrameryeast Nucleic Acid Structure II

  31. Histone deacetylation • Type III deacetylases usea non-trivial reaction:Prot-lys-NAc + NAD+ Prot-lys-NH3+ + nicotinamide +2’-O-acetyl-ADP-ribose • Part of the NAD salvage pathway Yeast Histone/protein deacetylase +histone H4 active peptide, 34kDaPDB 1SZD, 1.5Å Nucleic Acid Structure II

  32. Other histone PTM • Histones can be post-translationally modified in other ways as well • Methylation: e.g. lysines 4,27 of H3 • Phosphorylation: H2A phosphorylated at several sites near “hinge” • These are correlated with acetylation and play a role in folding and function Nucleic Acid Structure II

  33. How much does this coil up? • 200 bp extended would be about 50nm • The width of the core-particle disk is 5nm • So this is a tenfold reduction • Nucleosomal organization corresponds to negative supercoiling • … so DNA ends up supercoiled when we take away the histones Nucleic Acid Structure II

  34. Courtesy answers.com Next level of organization • H1 interacts with ~54 base-pairs of DNA along linker region • Individual histones spiral along to form 30 nm fiber • See fig.19.25 Courtesy Johns Hopkins Univ Nucleic Acid Structure II

  35. Even higher… • The 30nm fibers are attached to an RNA-protein scaffold that holds the 30nm fibers in large loops • Typical chromosome has ~200 loops • Loops are attached to scaffold at their base • Ends can rotate so it can be supercoiled Nucleic Acid Structure II

  36. What aboutprokaryotes? • No actual histones • Histone-like proteins(HLPs) involved • Bacterial DNA attached to scaffold in large loops (~100kb) • This makes a nucleoid Anabaena HU-DNA complex 33 kDa1P71, 1.9Å Nucleic Acid Structure II

  37. How many loops in bacteria? • Typical bacterial genome (E.coli) has 3000 open reading frames ~ 3000 genes. • Assume 500 amino acids per protein = 1500 bases per gene (ignores transcriptional elements) • Then genome is 1500 bp/gene * 3000 genes = 4.5*106 base-pairs • That’s (4.5*106 bp)/(1*105 bp/loop) = 45 loops Nucleic Acid Structure II

  38. iClicker question 1 • 1. Which of the following is a potential restriction site? • (a) ACTTCA • (b) AGCGCT • (c) TGGCCT • (d) AACCGG • (e) none of the above. Nucleic Acid Structure II

  39. iClicker question 2 • 2. A DNA sample has Tm=94ºC. It is probably • (a) AT-rich • (b) CG-rich • (c) characterized in the presence of chelators • (d) measured in pure water rather than buffer • (e) either (c) or (d) Nucleic Acid Structure II

  40. iClicker question 3 • 3. One step in gyrase activity depends on ATP hydrolysis. It is: • (a) association of the gyrase with the DNA loop • (b) DNA cleavage • (c) DNA re-ligation and release of DNA from gyrase • (d) all of the above Nucleic Acid Structure II

  41. iClicker question 4 • 4. When DNA is compressed, which of the compression steps accomplishes the most substantial reduction in size? • (a) helix to beads-on-a-string • (b) beads-on-a-string to solenoid • (c) solenoid to loop • (d) loop to 18-loop miniband • (e) 18-loop miniband to chromosome Nucleic Acid Structure II

  42. iClicker quiz, question 5 • 5. Suppose a mutation in the gene coding for histone H1 makes it fold up incorrectly. How will this mutation influence DNA organization? • (a) It will prevent formation of nucleosomes • (b) It will interfere with the beads-on-a-string organization between nucleosomes • (c) It will interfere with higher-level organization involving assembly of solenoids into loops • (d) All of the above • (e) None of the above Nucleic Acid Structure II

  43. iClicker question 6 • 6. When a histone becomes acetylated, the net charge on the protein • (a) goes up • (b) goes down • (c) does not change • (d) will go up or down depending on the circumstance Nucleic Acid Structure II

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