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Individual work. student of _____ group. Lesson 8 (II). Regulation of protein synthesis. Hereditary diseases. ⇐ ПредыдущаяСтр 6 из 6 Individual work student of _____ group _______________________________________________ (name) Lesson 8 (II). Regulation of protein synthesis. Hereditary diseases.
1. Name the main structural parts of operon, characterize their functions. ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ 2. What is the function of protein-repressor? What is the mechanism of its realization? ________________________________________________________________________________ ________________________________________________________________________________ 3. What functional states of repressor protein in inducible operon in: presence of inductor _______________________________________________________________ absence of inductor _______________________________________________________________ 4. What is the CAP-site of inducible operons? What is its function? ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ 5. Name known types of mutations, characterize changes in DNA and protein structure. 1) _____________________________________________________________________________ 2) _____________________________________________________________________________ 3) _____________________________________________________________________________ 4) _____________________________________________________________________________ 5) _____________________________________________________________________________ 6) _____________________________________________________________________________ 7) _____________________________________________________________________________ 6. Explane molecular changes in hemoglobin A that take place in sickle cell anemia. ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ 7. What are thevreasons of thalassemias? Name known variants of thalassemias. ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ 8. What positive effect of hemoglobinopathies for human population is possible? ________________________________________________________________________________ ________________________________________________________________________________ ________________________________________________________________________________ 9. Fill in the table "Inherited enzymopathies".
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