Genetics & Evolution Flashcards
(72 cards)
genetics
study of how traits are inherited from one generation to the next
genes
composed of DNA and are located on chromosomes
Mendel’s First Law (law of segregation)
- genes exist in alternative forms, a gene controls a specific trait
- organism has 2 alleles for each trait
- the 2 alleles segregate during meiosis, resulting in gametes that carry 1 allele
- if 2 alleles are different, 1 will be dominant, and the other will be recessive
Mendel’s Law of Dominance
dominant allele is expressed in the phenotype
Mendel’s Second Law (law of independent assortment)
- inheritance of one trait is completely independent of any other
- modern genetics: genes on the same chromosome will not follow this rule and will stay together unless crossing over occurs
incomplete dominance
- progeny phenotypes are blends of parental phenotypes
- heterozygote is an intermediate of the phenotypes of the homozygotes
codominance
- multiple alleles exist for a given gene and more than one of them is dominant
- ex: ABO blood groups, Ia and Ib are codominant and produce IaIb blood type
sex determination
- women have XX, men have XY
- gender of a zygote is determined by the contribution of the male gamete (if sperm carries and X or a Y)
- sex-linked: genes located on the X or Y chromosomes
sex linkage
- recessive genes carried on the X chromosome will produce the recessive phenotypes when they occur in men, ex: hemophilia and color blindness
- sex linked recessives generally affect only men, can be passed from grandfather to grandson via a daughter who is a carrier
nondisjunction
-failure of homologous chromosomes to separate properly during meiosis I or failure of sister chromatids to separate properly during meiosis II
trisomy
3 copies of a chromosome, ex: Down syndrome
monosomy
1 copy of a chromosome
chromosomal breakage
may occur spontaneously or by environmental factors such as mutagenic agents and X-rays
mutagenic agents
- induce mutations
- cosmic rays, X-rays, UV rays, and radioactivity, colchicine, or mustard gas
- sometimes also carcinogenic (cancer-causing)
point mutation
nucleic acid is replaced by another nuclei acid, affects between 1-3 nucleotides
silent mutation
the new codon codes for the same AA and no change is seen
missense mutation
new codon codes for a new AA, may or may not lead to problems in the resulting protein
nonsense mutation
new codon is a stop codon, lethal or severely inhibit the function
frameshift mutation
nucleic acids are deleted or inserted, often lethal bc it throw off entire sequence
examples of genetic disorders
- phenylketonuria (PKU): inability to produce the enzyme for the metabolism of phenylalanine
- sickle cell anemia: RBCs become crescent shaped, substitution of valine for glutamic acid
bacterial genome
- consists of a singular circular chromosome located in the nucleic region of the cell
- also contain smaller rings of DNA called plasmids
episomes
plasmids that are capable of integration into the bacterial genome
replication of bacterial chromosomes
- begins at a unique origin of replication and proceeds in both directions
- DNA is synthesized in the 5’-3’ direction
binary fission
- process by which bacterial cells reproduce
- asexual process