3.4 inheritance Flashcards
describe the methodology and conclusions drawn from mendels pea plant experiment
method:
mendel crossed pure breeding pea plants (P generation), then crossed large numbers of the offspring (F1)
he did this for a variety of different characteristics (flower color, plant height)
conclusions:
mendel concluded that organisms have discrete factors that control inheritance of traits (genes)
there are different versions of these factors (alleles) and each parent passes on one copy to the offspring
only one version gets expressed (dominance/ recessiveness)
explain how sexual reproduction results in diploid zygotes with two alleles for each characteristic
parents each pass on one copy of every chromosomes to offspring via haploid gametes
the resulting zygote is diploid and therefore possesses two copies of every gene
these alternative copies of a gene are called alleles
differentiate between homozygous, heterozygous and hemizygous
homozygous: alleles that are the same for a given characteristic
heterozygous: alleles are different for a given characteristic
homozygous: there is only one allele (occurs in males for sex chromosome traits)
distinguish between complete dominance and co dominance
complete dominance- one allele (dominant) masks expression of other allele (recessive) in heterozygotes
codominance- both alleles are expressed within a heterozygous phenotype
possible genotypes for the following blood groups
phenotype: type A
genotype: I^A I^A and I^A i
phenotype: type B
genotype: I I and I i
phenotype: type AB
genotype: I^A I^B
phenotype: type O
genotype: i i
identify which blood group is the universal donor and which is the universal acceptor
O is the universal donor
AB is the universal acceptor
define sex linkage and identify two examples of sex linked conditions
sex linkage refers to any gene/trait that is located on the sex chromosomes X or Y
two examples of X linked recessive conditions are hemophilia and red-green color blindness
outline why X linked recessive disorders are more common in males
males have only one X chromosome and so cannot be carriers for recessive conditions
describe the inheritance and cause of the following genetic diseases
cystic fibrosis:
-autosomal recessive disease
-caused by a mutation of the CFTR gene on chromosome 7
-causes the production of sticky mucus leading to obstructed airways and digestive issues
huntington’s disease:
-autosomal dominant disease
-caused by a mutation to the HTT gene on chromosome 4
-abnormal production of the Huntington protein leads to neuro degeneration and dementia
compare the health consequences associated with the Hiroshima bombing and chernobyl meltdown
chernobyl meltdown released more fissionable material with longer half lives
hiroshima bomb was detonated above ground and radiation was dispersed
hence, chernobyl responsible for more severe long term health effects such as cancer