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Lecture ten
Lecture ten

... 2. lacY gene = lactose permease – pumps lactose into the bacterial cell 3. lacA gene = thiogalactase transacetylase – function??? 4. lacI gene = codes for a lac repressor 5. operator = binds transcription factors 6. promoter = binds RNA polymerase ...
The science of replacing mitochondrial DNA and
The science of replacing mitochondrial DNA and

... Would a mother know if she were carrying mutations related to mitochondrial disorders? Does this really mean that a child born through The prevalence of maternally inherited MRT would have three parents? mitochondrial disorders is estimated to be roughly 1 in 5,000 adults. Some individuals who carry ...
Unit 3
Unit 3

... “brother.” Fraternal twins are like any brothers and sisters, except that they are born on the same day. They each have some the same genes as their parents. But they do not share an identical genetic makeup. Fraternal twins may resemble each other, but they usually will not be mistaken for each oth ...
translational - Bioinformatics Institute
translational - Bioinformatics Institute

... • DNase I footprinting assays identify protein-DNA interactions. • DNase I randomly hydrolyses phosphodiester bond. • Low concentration of DNase I used Æ on average each DNA molecule is cleaved just once. ...
Genetic Defects in Beef Cattle
Genetic Defects in Beef Cattle

No Slide Title
No Slide Title

... The ratio of the number of bp on each human chromosome covered by alignments of the reversed mouse genome and the number of base pairs covered by the actual mouse genome. ...
microbial genetics
microbial genetics

... copy number plasmids, there are enough plasmid molecules for each daughter cell to receive at least some (Fig.4a). The daughter cells do not have to inherit exactly half of the plasmid molecules. Thus, even if a daughter cell only receives a fewer copies of the plasmid than the copy number, this can ...
A simple and improved PCR-based technique for white
A simple and improved PCR-based technique for white

... each. However, finding copies of genes on both the X and Y chromosomes is difficult given the evolutionary loss of genetic material from the Y-chromosome (Vallender and Lahn 2004). The lack of recombination between mammalian X and Y chromosomes leads to different evolutionary histories and this dive ...
Biological information flow
Biological information flow

... Cis-acting element : DNA sequences that regulate expression of gene located on same DNA molecule Inr: initiator element ...
The C-terminus of S. pombe DDK subunit Dfp1 is
The C-terminus of S. pombe DDK subunit Dfp1 is

... cause the mutant to enter meiosis from either a haploid or a diploid state. While the haploid is frequently used as a meiotic model, the absence of homologous chromosomes and mating type heterozygosity leads to some differences in meiotic dynamics (Pankratz and Forsburg, 2005; Yamamoto and Hiraoka, ...
number of fifty human tumours
number of fifty human tumours

... cells are measured, it is nearly always found that the majority are grouped together, although the level of the mode varies widely in different tumours. A few cells may be expected to be synthesising DNA and to have values up to twice the "resting " value for this reason, but clearly these usually f ...
Agarose Gel Electrophoresis
Agarose Gel Electrophoresis

... large DNA fragments, as shown in Figure 2.5A.2B. For separating large DNA molecules, it is best to run gels at both low agarose concentrations and low applied voltages (∼1 V/cm, 0.5% agarose). Electrophoresis buffers. The two most widely used electrophoresis buffers are Tris/ acetate (TAE) and Tris/ ...
pdf
pdf

... host genome and do not kill the host, whereas lytic phage cause lysis of their hosts when they infect bacteria. The bacteriophage λ can choose between these two “lifestyles.” The molecular basis for this decision is one of the best understood genetic switches that has been studied, and it provides a ...
Mutation, Mutagens, and DNA Repair
Mutation, Mutagens, and DNA Repair

... In excision repair, the region of DNA containing the dimer or other damage is physically cut out and then replaced by new DNA synthesis (Figure 1). Excision repair has more steps and requires more enzymes than photoreactivation, but it can work on damage created by agents other than UV and on lesion ...
Additional file 5
Additional file 5

... probes. “Common” probes correspond to probes exhibiting true signals (>2 SD) in both strains (purple), while probes exhibiting true signals in one strain and not the other were considered as “strain-specific” (red and blue). Probes at the boundaries of the common and strain specific regions were des ...
Characterizing transcription factor binding sites using formaldehyde
Characterizing transcription factor binding sites using formaldehyde

... type of analysis is amenable to a larger range of fragment sizes than is gel mobility shift analysis. In place of cells containing stably integrated constructs, transiently transfected cells or cells containing episomes can also be used. All three of these methods (stably integrated plasmids, transi ...
64$ CfE Higher Biology Unit 1: DNA and the
64$ CfE Higher Biology Unit 1: DNA and the

... The significance of DNA and its role in hereditary can be traced from the work of Griffiths, who in 1928 demonstrated the "transforming principle" in bacteria. He, and later others (Avery, McCartney & McLeod, 1944), would show this "transforming principle" to be DNA. Later, in the 1950s, Hershey & C ...
CfE Higher Biology Unit 1: DNA and the Genome
CfE Higher Biology Unit 1: DNA and the Genome

... The significance of DNA and its role in hereditary can be traced from the work of Griffiths, who in 1928 demonstrated the "transforming principle" in bacteria. He, and later others (Avery, McCartney & McLeod, 1944), would show this "transforming principle" to be DNA. Later, in the 1950s, Hershey & C ...
Chapter 17
Chapter 17

... were the simplest viruses with small genomes. The first complete genome sequence of a free-living cellular organism was for the bacterium Haemophilus influenzae in 1995. ...
64$ CfE Higher Biology Unit 1: DNA and the
64$ CfE Higher Biology Unit 1: DNA and the

... The significance of DNA and its role in hereditary can be traced from the work of Griffiths, who in 1928 demonstrated the "transforming principle" in bacteria. He, and later others (Avery, McCartney & McLeod, 1944), would show this "transforming principle" to be DNA. Later, in the 1950s, Hershey & C ...
The Process of How COMT Genetic Variants Provide the
The Process of How COMT Genetic Variants Provide the

... (Morrow, 468). Individuals with the Warrior COMT gene generally have lower levels of dopamine than those who possess the Worrier gene due to the disparity between the catabolic rates of the COMT enzymes. Overall, COMT gene alleles predestine individuals to certain behavioral traits based on the amou ...
Mouse Repeats
Mouse Repeats

... the orthologous areas of the human genome than with the immediate GC-density (Waterston, Lindblad-Toh et al. 2002). This suggests that genomic features, which are correlated with but distinct from GC-content, may determine Alu/B1 distribution (Waterston, Lindblad-Toh et al. 2002). Like the B1 elemen ...
DNA Replication - Texas Tech University
DNA Replication - Texas Tech University

... Codes for proteins Can be modified by splicing, 5’ and 3’ additions ...
RNA polymerase I
RNA polymerase I

... When provided with a mixture of sugars, including glucose, the bacteria use glucose first. So long as glucose is present, operons such as lactose are not transcribed efficiently. Only after exhausting the supply of glucose does the bacterium fully turn on expression of the lac operon. Glucose exerts ...
CHAPTER ONE  INTRODUCTION 1
CHAPTER ONE INTRODUCTION 1

... Grand Naine banana cultivar “Novaria” (Roux, 2004). However, useful mutation occurs at a very low frequency and can affect other non targeted genes (Van Harten, 1998). In light of these limitations, genetic transformation that is considered to be precise in modifying traits of interest without alter ...
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Cre-Lox recombination



In the field of genetics, Cre-Lox recombination is known as a site-specific recombinase technology, and is widely used to carry out deletions, insertions, translocations and inversions at specific sites in the DNA of cells. It allows the DNA modification to be targeted to a specific cell type or be triggered by a specific external stimulus. It is implemented both in eukaryotic and prokaryotic systems.The system consists of a single enzyme, Cre recombinase, that recombines a pair of short target sequences called the Lox sequences. This system can be implemented without inserting any extra supporting proteins or sequences. The Cre enzyme and the original Lox site called the LoxP sequence are derived from bacteriophage P1.Placing Lox sequences appropriately allows genes to be activated, repressed, or exchanged for other genes. At a DNA level many types of manipulations can be carried out. The activity of the Cre enzyme can be controlled so that it is expressed in a particular cell type or triggered by an external stimulus like a chemical signal or a heat shock. These targeted DNA changes are useful in cell lineage tracing and when mutants are lethal if expressed globally.The Cre-Lox system is very similar in action and in usage to the FLP-FRT recombination system.
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