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S9. Computational Molecular Modeling
S9. Computational Molecular Modeling

... knowledge of how deletions of DNA base pairs in the DNA result in frameshift mutations at the protein level. If the instructor has not yet covered frameshift mutations in class it is probably best to complete this activity during the week 4 laboratory session rather than assign it as homework. Even ...
Genética Molecular em Medicina Transfusional
Genética Molecular em Medicina Transfusional

... primer: a small piece of single-stranded DNA 20-30 nt long that hybridizes to one strand of the template DNA. The rxn is intitiated by heating until the two strands of DNA separate, then the primers anneals to the complementary template strand, and DNA polymerase elongates the primer. ...
Chapter 7 Genes and Protein Synthesis
Chapter 7 Genes and Protein Synthesis

... missense and/or nonsense effects  Any deletion or insertion of base pairs in multiples of ...
Part I: To Transcribe! In previous lessons, you`ve learned the
Part I: To Transcribe! In previous lessons, you`ve learned the

... The segments of DNA that code for traits are called “genes.” The genes contain information that can be translated to mRNA and then transcribed into a protein. In other words, the genes found on DNA strands code for proteins. However, it is very important to note that not all of the genes in an organ ...
Oxygen (O 2 ) - Mona Shores Blogs
Oxygen (O 2 ) - Mona Shores Blogs

... This type of evolution has occurred when organisms look alike due to selection pressures of living in the same environment even though they do NOT come from a recent common ancestor. ...
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What is Willy Wonka famous for?

... imaginative technologies Willy Wonka created? ...
Transcription and translation
Transcription and translation

... • EPO boosts production of red blood cells – Lance Armstrong used it. • Concern now that athletes may inject genes to make EPO into their cells • New test can scan for this gene using introns/exons! • A person’s own EPO gene has introns. • An inserted gene would likely lack those introns. So their a ...
Lucerne Publishing F
Lucerne Publishing F

... DNA is a code for what our body needs to make to survive, such as proteins, enzymes, and hormones! Our DNA is organized into chromosomes. We have 23 chromosomes from each parent, so 46 in total! Every persons DNA is 99.9% similar to that of another person! It is the 0.1% differences that give us a u ...
Sem2 CA Bio Standards
Sem2 CA Bio Standards

... d. the central dogma of molecular biology outlines the flow of information from transcription of ribonucleic acid (RNA) in the nucleus to translation of proteins on ribosomes in the cytoplasm. ...
3rd Quarter Biology Assessment
3rd Quarter Biology Assessment

... 15) Place the following into the correct category on the Venn Diagram, referencing Figure 4: a. haploid (Meiosis) b. diploid (Mitosis) c. crossing over (Meiosis) d. two identical daughter cells (Meiosis) e. four different daughter cells (Meiosis) f. cell division process (Both) g. for repair and gr ...
TransformationSimulation
TransformationSimulation

... 17. Move the insulin gene to the open ends of the plasmid. Fit the insulin gene into the ring so the complimentary bases line up. When you are sure the base pairing is correct, tape the ends to create one new, closed ring. The enzymes that connect the pieces of DNA are called ligases. Scissors are u ...
Ch 12 Molecular Genetics
Ch 12 Molecular Genetics

... Ribosome moves down the mRNA so that the first tRNA is now in E-site of ribosome (and is released) A-site is now empty to attach the third tRNA carrying the third amino acid Steps 4-7 repeated until mRNA codon for stop is ...
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File

Lecture 14
Lecture 14

... pH when alkali was used to denature it, each strand will, after a time, find its complementary strand. The two strands will ‘zipper’ back together to re-form a double stranded DNA molecule. This ability of complementary sequences to anneal, or hybridize, to one another is called nucleic acid hybridi ...
Genetic Technology
Genetic Technology

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HNF4a Network - University of Wisconsin–Madison
HNF4a Network - University of Wisconsin–Madison

... (approximately 2 x 107 beta cells) were fixed and handled for HNF4a, HNF6, and RNA polymerase II. • HNF1a ChIP required significantly more material, typically 80,000 islets, to produce results with somewhat lower enrichment ratios than the results obtained with hepatocytes. • These results suggest t ...
(pt=4) Label the following diagram with the following terms: ATP
(pt=4) Label the following diagram with the following terms: ATP

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Enzymes - preabenagh
Enzymes - preabenagh

... Nucleic Acid Synthesis • Nucleotides joined by dehydration synthesis • Covalent bond forms between PHOSPHATE GROUP and SUGAR ...
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Thanksgiving Extra Credit Assignment

... 38. What is the error rate in DNA replication? What helps lower this error rate to 1 in 1 billion nucleotides? 39. What is a mutation? 40. Name several things that can cause DNA mutations. ...
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... • Single helix • Smaller than DNA • 5 carbon sugar = ribose • Uracil replaces thymine which binds with adenine ...
Causes
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... Enzymes Repair Damaged DNA • A human has 1014 nucleated cells each with 3x 109 base pairs of DNA. If about 1016 cell divisions occur in a lifetime and • 10−10 mutations per base pair per cell generation escape repair, • there may eventually be as many as one mutation per 106 bp in the genome. • For ...
DNA webquest
DNA webquest

... Click on the Animation button at the bottom. Click through the story using the arrow at the bottom right. When is new DNA made? ________________________________________________________________________ Why is DNA replication called “semi-conservative”? ________________________________________________ ...
Mutation
Mutation

... 2) UV light - favor GC -> AT - produces a photo dimer in adjacent thymine residues - abnormal base pairing 3) Aflotoxin - favors GC -> TA - generates apurinic sites by addition to N7 position of guanine (purine). 4) Base analogs - chemicals that are similar to normal bases - can be incorporated into ...
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Deoxyribozyme



Deoxyribozymes, also called DNA enzymes, DNAzymes, or catalytic DNA, are DNA oligonucleotides that are capable of catalyzing specific chemical reactions, similar to the action of other biological enzymes, such as proteins or ribozymes (enzymes composed of RNA).However, in contrast to the abundance of protein enzymes in biological systems and the discovery of biological ribozymes in the 1980s,there are no known naturally occurring deoxyribozymes.Deoxyribozymes should not be confused with DNA aptamers which are oligonucleotides that selectively bind a target ligand, but do not catalyze a subsequent chemical reaction.With the exception of ribozymes, nucleic acid molecules within cells primarily serve as storage of genetic information due to its ability to form complementary base pairs, which allows for high-fidelity copying and transfer of genetic information. In contrast, nucleic acid molecules are more limited in their catalytic ability, in comparison to protein enzymes, to just three types of interactions: hydrogen bonding, pi stacking, and metal-ion coordination. This is due to the limited number of functional groups of the nucleic acid monomers: while proteins are built from up to twenty different amino acids with various functional groups, nucleic acids are built from just four chemically similar nucleobases. In addition, DNA lacks the 2'-hydroxyl group found in RNA which limits the catalytic competency of deoxyribozymes even in comparison to ribozymes.In addition to the inherent inferiority of DNA catalytic activity, the apparent lack of naturally occurring deoxyribozymes may also be due to the primarily double-stranded conformation of DNA in biological systems which would limit its physical flexibility and ability to form tertiary structures, and so would drastically limit the ability of double-stranded DNA to act as a catalyst; though there are a few known instances of biological single-stranded DNA such as multicopy single-stranded DNA (msDNA), certain viral genomes, and the replication fork formed during DNA replication. Further structural differences between DNA and RNA may also play a role in the lack of biological deoxyribozymes, such as the additional methyl group of the DNA base thymidine compared to the RNA base uracil or the tendency of DNA to adopt the B-form helix while RNA tends to adopt the A-form helix. However, it has also been shown that DNA can form structures that RNA cannot, which suggests that, though there are differences in structures that each can form, neither is inherently more or less catalytic due to their possible structural motifs.
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