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Regulation of Gene Expression
Regulation of Gene Expression

... “Consider an individual E. coli cell living in the erratic environment of the human colon, dependent for its nutrients on the whimsical eating habits of the host.” “If the environment is lacking the amino acid tryptophan (which the bacterium needs to survive), the cell responds but activating a ...
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Transcription

... Protein synthesis involves two processes: transcription and translation.  In transcription the DNA message is converted into an mRNA molecule.  In translation the mRNA message is used to assemble amino acids into a protein chain. ...
Power Point Notes
Power Point Notes

... – Only small stretch is template – RNA polymerase catalyzes nucleotide addition – Product is a single strand of RNA ...
post-transcriptional gene silencing by double
post-transcriptional gene silencing by double

... the homologous endogenous gene. In fact, RNA viruses that replicate in the cytoplasm could provoke the production of small RNAs homologous to a gene fragment of their RNA genome. As stated above, silencing by PTGS/RNAi at one site in a plant or worm can spread throughout the organism. Small RNAs cou ...
Transcription and Translation Candy
Transcription and Translation Candy

... Make a model demonstrating the process of translation. Your model should include where in the cell translation takes place and the final product of translation. Your model should include the following: ribosomes, codons, tRNA with anti-codons and appropriate amino acid, forming polypeptide and compl ...
Test 4
Test 4

... A promoter may be present on either side of a gene or in the middle of it. B) All promoters have the same sequence that is recognized by RNA polymerase holoenzyme. C) Every promoter has a different sequence, with little or no resemblance to other promoters. D) Many promoters are similar and resemble ...
Microarray Data Analysis
Microarray Data Analysis

... • Fold change is often much greater for low intensity samples (absolute amount of RNA is small) • If you normalize by dividing all samples by the mean, then genes that express at this level will have their variation suppressed ...
Chem 465 Biochemistry II Hour Exam 3
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... Has a large CTD (carboxyterminal domain) that has several specialized functions not seen in Ecoli like sites to bind capping and splicing complexes. Will also have lots of interactions with other proteins as part of the more complex control mechanisms seen n eukaryotes. ...
26P PROCEEDINGS OF THE BIOCHEMICAL SOCIETY
26P PROCEEDINGS OF THE BIOCHEMICAL SOCIETY

... nucleic acid labelled in vivo, and attempts are now being made to find the sequence offragments of nonradioactive RNA, which are labelled at their 5'hydroxyl end with [32P]phosphate in vitro. This may be achieved by using a specific virus-induced phosphokinase and [y-32P]ATP. This may be the method ...
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... al. 1999). Two other family members, alg-1 and alg-2, functionally overlap and show strong developmental phenotypes, but are dispensable for RNAi in the soma (Cikaluk et al. 1999; Grishok et al. 2001). Drosophila contains four characterized Argonaute proteins (Piwi, Aubergine, dAgo1, and dAgo2) plus ...
Protein Synthesis Assign
Protein Synthesis Assign

... Objective: Students explore the process of protein synthesis and demonstrate an understanding of the various steps involved through the completion of one of the following activities. Introduction Protein synthesis is an essential process that occurs constantly within our cells. As you sit reading th ...
Identification of Genes Interacting with rnt-1 Through Large
Identification of Genes Interacting with rnt-1 Through Large

... overlapped expression of RUNX genes, regulation by upstream activators, numerous RUNX-targeted genes (Cohen 2009), and posttranscriptional regulations (Bae and Lee 2006) were identified for RUNX genes. In addition, RUNX proteins do not act alone, but in conjunction with cofactors; most RUNX proteins ...
AP Protein Synthesis
AP Protein Synthesis

... RNA processing1. 5' cap with a modified guanine nucleotide is added. 2. At the 3' end 30-200 adenine nucleotides are added (poly-Atail). -These modifications prevent the mRNA from being degraded and signal the ribosome where to attach. 3. There are noncoding regions (introns) that are removed in ...
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Transcription-Mediated Amplification
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... Second level of specificity: An isothermal amplification utilizing specific oligonucleotides further increases specificity and assay sensitivity. Transcription-Mediated Amplification (TMA) is an isothermal molecular amplification process utilizing two enzymes, reverse transcriptase (RT) and RNA poly ...
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Regulation of Transcription

... • In order for E. Coli to use (metabolise) the sugar a gene system referred to as the “lac operon” must produce three enzyme(s) that allow lactose to be utilised by the bacteria. For simplicity we will refer to the combined system as: lactose dehydrogenise (a more detailed description of the enzymes ...
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... Glycine insertion are pinpointed in the key features of the protein structure, strongly arguing for CSP-RNA nucleotide substitutions through or mediated via RNA editing and new residue insertion to produce new proteins with novel functions in pheromone synthesis [10] (Figure 1). ...
lesson viii - MisterSyracuse.com
lesson viii - MisterSyracuse.com

... specific sequence of bases. It signals the start of a gene. 12. RNA polymerase attaches here, and starts adding bases, using the DNA as a template strand. It is much slower than DNA polymerase, at only 40 bases per second. 13. It moves along until it hits the terminator. “You have been targeted for ...
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... The Binding of Amino Acids to Transfer RNAs • Aminoacyl-tRNA synthetases and tRNA charging • The specificity between an amino acid and its tRNA is determined by each individual aminoacyl-tRNA synthesis. • There are exactly 20 different aminoacyl-tRNA syntheses in a cell. Each synthetase recognizes ...
Protein Synthesis
Protein Synthesis

... code & carries the genetic information to the ribosomes • Ribosomal RNA (rRNA), along with protein, makes up the ribosomes • Transfer RNA (tRNA) transfers amino acids to the ribosomes where proteins are synthesized ...
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RNA interference



RNA interference (RNAi) is a biological process in which RNA molecules inhibit gene expression, typically by causing the destruction of specific mRNA molecules. Historically, it was known by other names, including co-suppression, post-transcriptional gene silencing (PTGS), and quelling. Only after these apparently unrelated processes were fully understood did it become clear that they all described the RNAi phenomenon. Andrew Fire and Craig C. Mello shared the 2006 Nobel Prize in Physiology or Medicine for their work on RNA interference in the nematode worm Caenorhabditis elegans, which they published in 1998.Two types of small ribonucleic acid (RNA) molecules – microRNA (miRNA) and small interfering RNA (siRNA) – are central to RNA interference. RNAs are the direct products of genes, and these small RNAs can bind to other specific messenger RNA (mRNA) molecules and either increase or decrease their activity, for example by preventing an mRNA from producing a protein. RNA interference has an important role in defending cells against parasitic nucleotide sequences – viruses and transposons. It also influences development.The RNAi pathway is found in many eukaryotes, including animals, and is initiated by the enzyme Dicer, which cleaves long double-stranded RNA (dsRNA) molecules into short double-stranded fragments of ~20 nucleotide siRNAs. Each siRNA is unwound into two single-stranded RNAs (ssRNAs), the passenger strand and the guide strand. The passenger strand is degraded and the guide strand is incorporated into the RNA-induced silencing complex (RISC). The most well-studied outcome is post-transcriptional gene silencing, which occurs when the guide strand pairs with a complementary sequence in a messenger RNA molecule and induces cleavage by Argonaute, the catalytic component of the RISC complex. In some organisms, this process spreads systemically, despite the initially limited molar concentrations of siRNA.RNAi is a valuable research tool, both in cell culture and in living organisms, because synthetic dsRNA introduced into cells can selectively and robustly induce suppression of specific genes of interest. RNAi may be used for large-scale screens that systematically shut down each gene in the cell, which can help to identify the components necessary for a particular cellular process or an event such as cell division. The pathway is also used as a practical tool in biotechnology, medicine and insecticides.
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