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Molecular medicine: Promises and patience
Molecular medicine: Promises and patience

... with Duchenne’s muscular dystrophy administration of small strands of ologonucleotides interfered with mRNA splicing and corrected the reading frame by exon skipping of the mutated part of the dystrophin gene, causing a truncated (but biologically active) gene product rather than the inactive mutant ...
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... DNA-binding domain is to bring the activation domain into the vicinity of the startpoint. And activation is independent of the means of tethering. we can think of DNA-binding (or RNA-binding in the case of tat) domain as providing a "tethering" function, whose main purpose is to ensure that the act ...
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Bill Nye Genes Video WKSHT
Bill Nye Genes Video WKSHT

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Name Date “Bill Nye: Genes” Video Worksheet 1. Where do your
Name Date “Bill Nye: Genes” Video Worksheet 1. Where do your

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Transcription - Dr. Salah A. Martin

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... based in the 5’nuclease activity of Taq polymerase. When the probes are intact, the quencher interacts with the fluorophore by FRET, quenching their fluorescence. one probe is complementary to the wild-type allele and the other to the variant allele. These probes have different fluorescent dyes atta ...
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Sequence Alignment 1

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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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