Functional cloning
You don't need to be Editor-In-Chief to add or edit content to WikiDoc. You can begin to add to or edit text on this WikiDoc page by clicking on the edit button at the top of this page. Next enter or edit the information that you would like to appear here. Once you are done editing, scroll down and click the Save page button at the bottom of the page.
Functional cloning involves using a known gene sequence as a probe to look for new gene sequences that may have similar functions, based on the similarity of sequence. Using this method of analysis, researchers can search through entire genomes to find genes of interest without having prior knowledge of their location. The genes, once putatively identified, can then be tested to see if their function is in fact similar to the initial gene of interest. This technique is useful when a given pathway or enzyme is present in one organism, and one wishes to identify the presence of a similar pathway or enzyme in a different organism.
Phage expression libraries can be screened using probes designed based on the gene of interest.[1]
Contents |
Functional cloning versus positional cloning
“One way to conceptualize the difference between functional and positional cloning is to consider methods for looking up words. Functional cloning is akin to using a thesaurus to look up a known word and thereby to select new words with related meanings (or functions). Positional cloning is similar to reading though a specific page of a dictionary, browsing for interesting words of any meaning located on that page. In the first case, words and genes are selected for their function, be it in a sentence or in a cell. In the second case, words and genes are selected for position regardless of their function.”[1]
See also
References
External links
- Functional Cloning, Sorting, and Expression Profiling of Nucleic Acid-Binding Proteins Genome Research.com
- A novel strategy for the functional cloning of enzymes using filamentous phage display: the case of nucleotidyl transferases Oxford Journals]
- Molecular genetics of Cohen syndrome Department of Medical Genetics, University of HelsinkiTemplate:Biotech-stub
Acknowledgement and Attribution Regarding Sources of Content
Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .

