Hall: Guyton and Hall Textbook of Medical Physiology, 12th Edition Chapter 03: Genetic Control of Protein Synthesis, Cell Function, and Cell Reproduction Test Bank 1. Facioscapulohumeral muscular dystrophy (FSHD) is characterized by the deletion of a DNA sequence on chromosome 4q35. This deletion correlates with both the inability of a specific protein complex to bind to the DNA and an overexpression of the genes upstream of the deletion. The sequence deleted in FSHD most likely functions normally as: A. An activator protein B. C. D. E.
A repressor protein An activator element A repressor element A promoter sequence
E. Translation is initiated by small ribosomal subunits anchored to the ER membrane; protein is glycosylated in the Golgi apparatus; the protein is packaged into lysosomes ANS: C
A. Multiple ribosomes can simultaneously translate a single mRNA molecule B. Each codon codes for one amino acid C. One mRNA molecule can code for multiple proteins, depending on which start codon is recognized by the small ribosomal subunit D. Translation is terminated when the release factor binds to the stop codon ANS: C
E. Protein glycosylation ANS: B 13. The appearance of which of the following distinguishes eukaryotic cells from lower units of life like bacteria and viruses? A. DNA B. RNA C. Membranes D. Protein E. Nucleus ANS: E
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