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PDF LECTURE 8: Genetic dissection of biochemical pathways

We now know that the biochemical pathway is as follows: Phenylalanine --> Tyrosine --> p-Hydroxyphenylpyruvate --> 25-Dihydroxyphenylpyruvate --> Homogentisic Acid --> Maleylacetoacetic Acid --> --> --> CO2 + H20 Other mutations causing human disease in this metabolic pathway include: Phenylketonuria (PKU): mutation in phenylalanine hydoxylase

  • What is a biosynthetic pathway?

    When different genes function in different sequential steps of a biological process, this is known as a genetic pathway. Perhaps the most conceptually intuitive type of pathway is a biosynthetic pathway, where a precursor molecule is chemically modified through a series of enzymatically catalyzed intermediate steps to produce a bioactive product.

  • How can genetics be used to study biochemistry?

    In effect, this session outlines how genetics can be used to study biochemistry. It includes a discussion of yeast as a model system. It outlines how to identify mutants with mutations in the same pathway, how to characterize the mutants into complementation groups, and how to use epistasis tests to infer details about a biochemical pathway.

  • How do we identify genes that affect a particular biological process?

    One way to identify genes that affect a particular biological process is to induce random mutations in a large population, and then look for mutants with phenotypes that might be caused by a disruption of a particular biochemical pathway.

Biochem Pathway Analysis part 1

Biochem Pathway Analysis part 1

Catecholamine Biosynthesis Pathway

Catecholamine Biosynthesis Pathway

Biochemical Pathway Analysis part 2

Biochemical Pathway Analysis part 2

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