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DNA, RNA, and the Flow of Genetic Information
DNA, RNA, and the Flow of Genetic Information

... next. These macromolecules consist of a large number of linked nucleotides, each composed of a sugar, a phosphate, and a base. Sugars linked by phosphates form a common backbone that plays a structural role, whereas the sequence of bases along a nucleic acid chain carries genetic information. The DN ...
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... mutated (GeneB) genes; this is known as a DNA sequence alignment. An alignment uses an algorithm (a step-by-step procedure) to compare the order of nucleotide bases in the sequences and then lines them up so that the number of identical bases is maximized. The alignment program will point out those ...
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... paternal chromosomes). Another student in your lab tells you that only one-fourth of the gametes produced by meiosis in this parasite will have all of it’s chromosomes from either maternal or paternal origin (i.e. all the chromosomes from dad or all the chromosomes from mom). Assume that meiosis in ...
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... Although Rot analysis can be used to reveal the complexity of mRNA population in any cell type, the number of gene expressed in any cell type can be determined by DNA microarray. In this assay, the mRNA isolated from the cell type of interest can be reversed transcribed to cDNA with tags The labeled ...
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... • Make genomic library from mutant – What type of library will you make? Why? • Screen with transposon – Recover positives, sequence flanking region • Use flanking sequence to screen normal genomic library – What type of library will you screen? – If insertion is a gene trap or related • You can dig ...
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... Other reporter genes: • Artificial vectors with restriction sites within the lac operon. If new DNA is ...
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Genomic library



A genomic library is a collection of the total genomic DNA from a single organism. The DNA is stored in a population of identical vectors, each containing a different insert of DNA. In order to construct a genomic library, the organism's DNA is extracted from cells and then digested with a restriction enzyme to cut the DNA into fragments of a specific size. The fragments are then inserted into the vector using DNA ligase. Next, the vector DNA can be taken up by a host organism - commonly a population of Escherichia coli or yeast - with each cell containing only one vector molecule. Using a host cell to carry the vector allows for easy amplification and retrieval of specific clones from the library for analysis.There are several kinds of vectors available with various insert capacities. Generally, libraries made from organisms with larger genomes require vectors featuring larger inserts, thereby fewer vector molecules are needed to make the library. Researchers can choose a vector also considering the ideal insert size to find a desired number of clones necessary for full genome coverage.Genomic libraries are commonly used for sequencing applications. They have played an important role in the whole genome sequencing of several organisms, including the human genome and several model organisms.
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