Patho I Flashcards
(75 cards)
Codon
genetic code that is determined by a sequence of three consecutive bases.
DNA is composed of
of a double stranded, helical structure of nucleotides
ATGC
what codons signals STOP
UGA (Uracil-Guanine-Adenine)
t/f: A gene typically codes for one specific protein or functional RNA, not multiple types
true
t/f: Each daughter cell has the same number of chromosomes as the parent cell in mitosis
true
Describes cell division that gives rise to reproductive cells with half the number of chromosomes of the mother
Meiosis
cell division that creates two daughter cells
Mitosis
t/f: Mitosis occurs in somatic (body) cells, not germ cells
true
t/f: Anticodon of tRNA aligns with an mRNA codon to properly sequence amino acids and chemically bond them
true
t/f: DNA is transcribed into mRNA, which exits the nucleus and is translated into protein in the cytoplasm
true
t/f: anticodon of tRNA aligns with the codon on mRNA
true
t/f: Thymine (T) in DNA is replaced by Uracil (U) in RNA
true
locus
physical location of a gene on a chromosome
Punnett Square
diagram used to predict the genotypes of offspring from parent allele combinations
Phenotype
observable characteristics or traits of an organism
Cystic fibrosis
- autosomal recessive disorder, requiring two defective copies of the gene
- result of an autosomal recessive disorder, meaning that the child must inherit two defective copies of the gene from each parent
- The disease is present at the time of birth
- May result in poor nutrition and liver disease, due to mucus clogging
- Susceptibility to lung infection increases due to mucus clogging
t/f: A carrier mother has a 50% chance of passing the defective gene to sons (who would be affected) and a 50% chance of passing it to daughters (who would become carriers)
true
t/f: Fathers cannot pass X-linked traits to sons, since sons inherit their X chromosome from their mother
true
t/f: An affected father will always pass the X-linked gene to all daughters; if dominant, all daughters will be affected
true
Trisomy 21 (Down Syndrome)
- Excess skin at the nape of the neck is a common symptom
- There is a long-term risk of leukemia and Alzheimer’s
- Decrease in muscle tone at birth (hypotonia) is common
- Cardiovascular and gastrointestinal defects are frequently present
Teratogenic Agents
- Irradiation may damage cells and result in microcephaly
- The most vulnerable time is during organogenesis
- Teratogenic agents are substances that cause malformations
- Drugs that cross the placenta can damage the embryo
Essential to prevent Spina Bifida
Folic Acid (B9)
Prenatal Screening
Second trimester blood work can screen for genetic or birth defects
Cellular Metaplasia
Conversion of one adult cell to another type of cell