Chemical Sructru of Nucleotide

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Chemical structure of nucleotide

 Introduction ➨ Deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) are the molecules that carry genetic information in the cell ★ DNA is the molecular archive for protein synthesis ★ RNA molecules transcribe and translate the information from DNA so it can be

used to direct protein synthesis

➨ DNA is comprised of two polymer strands held together by hydrogen bonds ★ Its overall structure is that of a twisted ladder ★ The sides of the ladder are alternating sugar and phosphate units ★ The rungs of the ladder are hydrogen-bonded pairs of heterocyclic amine bases

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➨ DNA polymers are very long molecules ★ DNA is supercoiled and bundled into 23 chromosomes for packaging in the cell

nucleus

➨ The sequence of heterocyclic amine bases in DNA encodes the genetic information required to synthesize proteins ★ Only four different bases are used for the code in DNA ★ A section of DNA that encodes for a specific protein is called a gene ★ The set of all genetic information coded by the DNA in an organism is its genome ★ The set of all proteins encoded in the genome of an organism and expressed at

any given time is its proteome

➨ The sequence of the human genome is providing valuable information related to human health ★ Example: A schematic map of genes on chromosome 19 that are related to

disease

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 Nucleotides and Nucleosides ➨ Mild degradation of nucleic acids yields monomer units called nucleotides ➨ Further hydrolysis of a nucleotide yields: ★ A heterocyclic amine base ★ D-ribose (from RNA) or 2-deoxy-D-ribose (from DNA); both are C5 monosaccharides ★ A phosphate ion

➨ The heterocylic base is bonded by a β N-glycosidic linkage to C1’ of the monosaccharide ★ Examples: A general structure of an RNA nucleotide (a) and adenylic acid (b)

➨ A nucleoside is a nucleotide without the phosphate group ★ A nucleoside of DNA contains 2-deoxy-D-ribose and one of the following four bases

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➨ A nucleoside of RNA contain the sugar D-ribose and one of the four bases adenine, guanine, cytosine or uracil

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➨ Nucleosides that can be obtained from DNA

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➨ Nucleosides that can be obtained from RNA

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➨ Nucleotides can be named in several ways ★ Adenylic acid is usually called AMP (adenosine monophosphate) ★ It can also be called adenosine 5’-monophosphate or 5’-adenylic acid

➨ Adenosine triphosphate (ATP) is an important energy storage molecule ➨ The molecule 3’,5’-cyclic adenylic acid (cyclic AMP) is an important regulator of hormone activity ★ This molecule is biosynthesized from ATP by the enzyme adenylate cyclase

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 Laboratory Synthesis of Nucleosides and

Nucleotides ➨ Silyl-Hilbert-Johnson Nucleosidation ★ An N-benzoyl protected base reacts with a benzoyl protected sugar in the

presence of tin chloride and BSA (a trimethylsilylating agent) ★ The trimethylsilyl protecting groups are removed with aqueous acid in the 2nd step ★ The benzoyl groups can be removed with base

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➨ Unnatural nucleotide derivatives can be synthesized from nucleosides bearing a substitutable group on the heterocyclic ring

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➨ Dibenzyl phosphochloridate is a phosphorylating agent for converting nucleosides to nucleotides

★ The 5’-OH is phosphorylated selectively if the 2’- and 3’-OH groups are protected

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 Deoxyribonucleic Acid: DNA  Primary Structure ➨ The monomer units of nucleic acids are nucleotides ★ Nucleotides are connected by phosphate ester linkages

➨ The backbone of nucleic acids consists of alternating phosphate and sugar units ➨ Heterocyclic bases are bonded to the backbone at each sugar unit ➨ The base sequence contains the encoded genetic information ➨ The base sequence is always specified from the 5’ end of the nucleic acid

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 Secondary Structure ➨ The secondary structure of DNA was proposed by Watson and Crick in 1953 ➨ E. Chargaff noted that in DNA the percentage of pyrimidine bases was approximately equal to the percentage of purine bases ★ Also the mole percentage of adenine Is nearly equal to that of thymine ★ The mole percentage of guanine is nearly equal to cytosine

➨ Chargaff also noted that the ratio of A and T versus G and C varies by species but the ratio is the same for different tissues in the same organism

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➨ X-ray crystallographic data showed the bond lengths and angles of purine and pyrimidine bases ★ X-ray data also showed DNA had a long repeat distance (34 Å)

➨ Based on this data, Watson and Crick proposed the double helix model of DNA (next slide) ★ Two nucleic acid chains are held together by hydrogen bonding between the ★ ★ ★ ★

bases on opposite strands The double chain is wound into a helix Each turn in the helix is 34Å long and involves 10 successive nucleotide pairs Each base pair must involve a purine and a pyrimidine to achieve the proper distance between the sugar-phosphate backbones Base pairing can occur only between thymine and adenine, or cytosine and guanine; no other pairing has the optimum pattern of hydrogen bonding or would allow the distance between sugar-phosphate backbones to be regular

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➨ Specific pairing of bases means the two chains of DNA are complementary ★ Knowing the sequence of one chain allows one to also know the sequence of the

other

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 Replication of DNA (see next slide) ➨ The DNA strand begins to unwind just prior to cell division ➨ Complementary strands are formed along each chain (each chain acts as a template for a new chain) ➨ Two new DNA molecules result; one strand goes to each daughter cell

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 RNA and Protein Synthesis ➨ “The central dogma of molecular genetics”

➨ A gene is the portion of a DNA molecule which codes for one protein ★ Proteins have many critical functions, e.g., catalysis, structure, motion, cell

signaling, the immune response, etc.

➨ DNA resides in the nucleus and protein synthesis occurs in the cytoplasm ★ Transcription of DNA into messenger RNA (mRNA) occurs in the nucleus ★ mRNA moves to the cytoplasm and the translation into proteins occurs using two

other forms of RNA: ribosomal RNA (rRNA) and transfer RNA (tRNA)

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 Transcription: Synthesis of Messenger RNA (mRNA) ➨ In the nucleus a DNA molecule partially unwinds to expose a portion corresponding to at least one gene ➨ Ribonucleotides with complementary bases assemble along the DNA strand ★ Base-pairing is the same in RNA, except that in RNA uracil replaces thymine

➨ Ribonucleotides are joined into a chain of mRNA by the enzyme RNA polymerase

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➨ An intron (intervening sequence) is a segment of DNA which is transcribed into mRNA but not actually used when a protein is expressed ➨ An exon (expressed sequence) in the part of the DNA gene which is expressed ➨ Each gene usually contains a number of introns and exons ★ Introns are excised from mRNA after transcription

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 Ribosomes - rRNA ➨ Protein synthesis is catalyzed in the cytoplasm by ribosomes ★ A ribosome consists of approximately two thirds RNA and one third protein ★ A ribosome is a ribozyme ( an reaction catalyst made of ribonucleic acid)

➨ A ribosome has 2 large subunits ★ The 30S subunit binds the mRNA that codes for the protein to be translated ★ The 50S subunit catalyzes formation of the amide bond in protein synthesis

➨ Transfer of an amino acid to the growing peptide chain is aided by acid-base catalysis involving an adenine in the 50S subunits

➨See Figure 25.14, page 1238

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 Transfer RNA (tRNA) ➨ Transfer RNAs (tRNAs), specific to each amino acid, transport amino acids to complimentary binding sites on the mRNA bound to the ribosome ★ More than one tRNA codes for each amino acid

➨ tRNA is comprised of a relatively small number of nucleotides whose chain is folded into a structure with several loops ★ One arm of the tRNA always terminates in the sequence cytosine-cytosine-

adenine, and it is here the amino acid is attached ★ On another arm is a sequence of three bases called the anticodon, which binds with the complementary codon on mRNA

➨ The mRNA genetic code is shown on the next page ➨ The structure of a tRNA molecule is shown in Figure 25.15, page 1240

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 The Genetic Code ➨ The genetic code is based on three-base sequences in mRNA ➨ Each three-base sequence corresponds to a particular amino acid ★ The fact that three bases are used to code for each amino acid provides

redundancy in the overall code and in the start and stop signals ★ N-formyl methionine (fMet) is the first amino acid incorporated into bacterial protein and appears to be the start signal ★ fMet is removed from the protein chain before its synthesis is complete

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 Translation ➨ Translation is peptide synthesis by a ribosome using the code from an mRNA ➨ The following is an example (see figure on next page): ★ An mRNA binds to a ribosome ★ A tRNA with the anticodon for fMet associates with the fMet codon on the mRNA ★ A tRNA with anticodon UUU brings a lysine residue to the AAA mRNA codon ★ The 50S ribosome catalyzes amide bond formation between the fMET and lysine ★ The ribosome moves down the mRNA chain to the next codon (GUA) ★ A tRNA with the anticodon CAU brings a valine residue ★ The ribosome catalyzes amide bond formation between Lys and Val ★ The ribosome moves along the mRNA chain and the process continues, e.g., with

the tRNA for phenylalanine binding to the ribosome ★ A stop signal is reached and the ribosome separates from the mRNA ★ At this point the polypeptide also separates from the ribosome

➨ The polypeptide begins to acquire its secondary and tertiary structure as it is being synthesized ➨ Several ribosomes can be translating the same mRNA molecule simultaneously ➨ Protein molecules are synthesized only when they are needed ★ Regulator molecules determine when and if a particular protein will be expressed

i.e. synthesized

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 Determining the Base Sequence of DNA ➨ The Chain-Terminating (Dideoxynucleotide) Method ★ DNA molecules are replicated in such a way that a family of partial copies is

generated; each DNA copy differs in length by only one base ★ Random chain-termination is done by ‘poisoning’ a replication reaction with a low concentration of 2’3’-dideoxynucleotides, which are incapable of chain elongation at their 3’ position ★ The 2’3’-dideoxynucleotides are labeled with covalently attached colored fluorescent dye molecules, with each color representing a base type

★ The partial copies are separated according to length by capillary electrophoresis ★ The terminal base on each strand is detected by the color of laser-induced

fluorescence as each DNA molecule passes the detector ★ A four-color chromatogram is generated (see Figure 25.17, page 1246)

➨ Automation of high-throughput ‘dideoxy’ sequencing made possible completion of the Human Genome Project by the 50th anniversary of Watson and Crick’s elucidation of the structure of DNA in 2003 Chapter 25

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 Laboratory Synthesis of DNA ➨ Solid-phase methods for laboratory synthesis of DNA are similar to those used for laboratory synthesis of proteins ★ The solid phase is often controlled-pore glass (CPG) ★ Protecting/blocking reagents are needed (e.g., the dimethoxytrityl and β -cyanoethyl

groups) ★ A coupling reagent (1,2,3,4-tetrazole) is used to join the protected nucleotides

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 The Polymerase Chain Reaction (PCR) ➨ PCR is an extraordinarily simple and effective method for exponentially multiplying (amplifying) the number of copies of a DNA molecule. ★ PCR beginning with a single molecule can lead to 100 billion copies in an afternoon ★ The Nobel Prize was awarded to K. Mullis in 1993 for invention of PCR

➨ PCR requires: ★ A sample of the DNA to be copied ★ The enzyme DNA polymerase ★ A short ‘primer’ sequence complimentary to the template DNA ★ A supply of A, C, G, and T nucleotide triphosphate monomers ★ A simple device for thermal cycling during the reaction sequence

➨ The PCR process is summarized on the next 2 slides

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