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BIOL 133 Ch. 5 Questions with answer
Typology: Exams
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The different forms of Leber congenital amaurosis arise because there are many ways that a mutation can disrupt the functioning of the rods and cones, the cells that provide vision. This best describes what phenomenon? ✔Genetic heterogeneity The Bombay phenotype is a result of ____ interacting genes and is an example of ____. ✔2; epistasis Different alleles that are both expressed in a heterozygote are _______. ✔codominant Mendel's laws can appear to not operate when one gene masks or otherwise affects the phenotype of another. This phenomenon is called _________. ✔epistasis The mutation that causes achondroplastic dwarfism is in the gene that encodes a receptor for a(n) ✔growth factor In ______ dominance, the heterozygous phenotype is intermediate between that of either homozygote ✔incomplete When all mitochondria bear the mutant allele, it is called ________ ✔homoplasmy A compound heterozygote is an individual ✔with two different mutant alleles for the same gene A(n) _________ is a molecule that the immune system recognizes and responds to ✔antigen 24 of the 37 genes of the mitochondrion encode ______ molecules that help assemble proteins. The other 13 genes encode proteins that function in cellular _______, which is the process that uses energy from digested nutrients to synthesize ATP.
✔RNA; respiration Which of the following is a true statement about a lethal genotype? ✔It causes death before an individual can reproduce. Mutations in which of the following genes are responsible for Marfan syndrome? ✔Fibrillin and transforming growth factor beta receptor Identify a disease that is both incompletely penetrant and variably expressive ✔Polydactyly Identify the symptoms of mitochondrial myopathies ✔Great fatigue, weak and flaccid muscles, and intolerance to exercise A blood type called the Bombay phenotype illustrates ___________ ✔epistasis The limb birth defect caused by the drug ________ is a phenocopy of the rare inherited illness phocomelia ✔thalidomide When both parents carry a recessive lethal allele for the same gene, each pregnancy has a ________ chance of spontaneously aborting ✔25% In humans, the dominance relationship between the A and B alleles of the ABO blood group gene is an example of ________ ✔codominance An individual with two different mutant alleles for the same gene is called a
✔compound heterozygote Marfan syndrome is caused by a mutation in the gene that codes for a protein called __________. This protein is abundant in the lens of the eye, in the aorta, and in the bones of the limbs, fingers, and ribs. ✔fibrillin In humans, mitochondrial DNA typically exhibits
In a blood type called the Bombay phenotype, the ________ gene controls the placement of a molecule to which antigens A and B attach on red blood cell surfaces. ✔H DNA in the mitochondria ✔does not crossover and mutates faster than DNA in the nucleus An infection can be a phenocopy if it affects ________ ✔more than one family member True or false: For Tay-Sachs disease, the heterozygote has the same level of enzyme as the homozygous dominant individual ✔false Blood types are determined by the patterns of molecules on the surfaces of ✔red blood cells What do diseases resulting from mutations in mitochondrial diseases affect? ✔Both mitochondrial protein synthesis and cellular energy reactions All of the following are features of mitochondrial DNA EXCEPT: ✔one copy per mitochondrion An underweight child who has frequent colds may show some signs of cystic fibrosis, but may instead suffer from malnutrition. This best describes what concept? ✔Phenocopy Leigh syndrome is caused by a mutation in a ________ gene and it affects the
✔mitochondrial; central nervous system A woman who does not have a mitochondrial disease can _________ ✔still pass the associated condition to a child, provided she is heteroplasmic