Chapter 21: Problem 18
What are gene microarrays? How are microarrays used?
Chapter 21: Problem 18
What are gene microarrays? How are microarrays used?
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Get started for freeGenomic sequencing has opened the door to numerous studies that help us understand the evolutionary forces shaping the genetic makeup of organisms. Using databases containing the sequences of 25 genomes, scientists (Kreil, D.P. and Ouzounis, C.A., Nucl. Acids Res. 29: \(1608-1615,2001\) ) examined the relationship between GC content and global amino acid composition. They found that it is possible to identify thermophilic species on the basis of their amino acid composition alone, which suggests that evolution in a hot environment selects for a certain whole organism amino acid composition. In what way might evolution in extreme environments influence genome and amino acid composition? How might evolution in extreme environments influence the interpretation of genome sequence data?
In what way will the discipline called metagenomics contribute to human health and welfare?
Archaea (formerly known as archaebacteria) is one of the three major divisions of living organisms; the other two are eubacteria and eukaryotes. Nanoarchaeum equitans is in the Archaea domain and has one of the smallest genomes known, about 0.5 Mb. How can an organism complete its life cycle with so little genetic material?
What is bioinformatics, and why is this discipline essential for studying genomes? Provide two examples of bioinformatics applications.
Comparisons between human and chimpanzee genomes indicate that a gene that may function as a wild type or normal gene in one primate may function as a disease-causing gene in another (The Chimpanzee Sequence and Analysis Consortium, Nature, \(437: 69-87,2005\) ). For instance, the \(P P A R G\) locus (regulator of adipocyte differentiation) is associated with type 2 diabetes in humans but functions as a wild-type gene in chimps. What factors might cause this apparent contradiction? Would you consider such apparent contradictions to be rare or common? What impact might such findings have on the use of comparative genomics to identify and design therapies for disease-causing genes in humans?
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