Test 1 Study Guide Flashcards

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1
Q

Model organisms in genetics

A

short generation time, easy to maintain and grow in restricted space, easy to provide necessary nutrients for growth, well-understood development and growth, closely resemble other organisms or systems

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2
Q

Watson & Crick

A

B-DNA, right-handed helical structure of DNA that exists when water is abundant; the secondary structure described by ____ & ____ and the most common DNA structure in cells

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3
Q

Mendel

A

“father of genetics”; pea plant experiments lead to the discovery of fundamental principles of inheritance (concepts of dominant and recessive traits), laws of segregation, independent assortment

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4
Q

Gilbert & Sanger

A

discovered the exact sequence of the nucleotide building blocks in DNA

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5
Q

Morgan & Sutton

A

Morgan: using fruit flies, he discovered a mutation affecting eye color allowing him to demonstrate how specific traits are linked to specific chromosomes

Sutton: chromosomes are the basis of heredity, reduction of chromosomes in meiosis is directly related to law of inheritance

= chromosome theory

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6
Q

Allele frequency of a population

A

how common an allele is in a population;

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7
Q

Sub-disciplines of genetics

A

molecular genetics, population genetics, transmission genetics (classical genetics), quantitative genetics, and developmental genetics

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8
Q

Errors in chromosome separation/ nondisjunction

A

when chromosomes fail to separate properly during cell division, resulting in daughter cells with an abnormal number of chromosomes, often leading to genetic disorders like Down syndrome

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9
Q

Significance of G2/M phase

A

checkpoint in the cell cycle near the end of G2; after this checkpoint has been passed, the cell undergoes mitosis; prevents cells from entering mitosis when DNA is damaged, providing an opportunity for repair and stopping the proliferation of damaged cells

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10
Q

Significance of G1/S phase

A

checkpoint in the cell cycle near the end of G1; after this checkpoint has been passed, DNA replicates, and the cell is committed to dividing

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11
Q

Significance of SRY in humans

A

sex-determining region Y; the male determining gene in mammals located on the Y chromosome

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12
Q

Sex linked inheritance

A

the process by which genes on sex chromosomes are passed down from parents to their offspring. In humans, sex-linked traits are usually associated with the X chromosome, which has more genes than the Y chromosome
EX: colorblindness

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13
Q

ZZ & ZW sex chromosomes

A

ZZ = males, ZW = females
in birds

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14
Q

XX & XY sex chromosomes

A

XX = female, XY = male
in humans

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15
Q

X and Y linked genetic disorders and inheritance pattern

A

X-linked genetic disorders are inherited through the X chromosome, meaning males are more likely to be affected due to only having one X chromosome, while Y-linked disorders are only passed from father to son as the Y chromosome is only present in males; both types of disorders exhibit distinct inheritance patterns based on the sex chromosomes involved

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16
Q

Blood group inheritance pattern

A

codominance

17
Q

Transmission genetics

A

field of genetics that encompasses the basic principles of heredity and how traits are passed from one generation to the next

18
Q

Genome

A

complete set of genetic instruction for any organism

19
Q

Phenotype

A

appearance or manifestation of a characteristic

20
Q

Genotype

A

the set of alleles possessed by an individual organism

21
Q

Mutations

A

heritable change in genetic information

22
Q

Allele

A

one of two or more alternative forms of a gene

23
Q

Centromere

A

constricted region on a chromosome that stains less strongly than the rest of the chromosome; serves as the attachment point for spindle microtubules

24
Q

Double fertilization

A

fertilization in plants; includes the fusion of a sperm cell with an egg cell to form a zygote and the fusion of a second sperm cell with the polar nuclei to form an endosperm

24
Q

Telomere

A

stable end of a eukaryotic chromosome

25
Q

Barr body

A

inactivated X chromosome that appears as a condensed, darkly staining body in the nuclei of most cells of female placental mammals

25
Q

Test cross

A

a breeding experiment that determines the genotype of an organism by crossing it with a homozygous recessive organism

26
Q

Polydactyly

A

a condition where someone has more than 5 toes or fingers

27
Q

Variable expressivity

A

a genetic phenomenon where individuals with the same genetic condition have different signs and symptoms

28
Q

Lethal alleles

A

allele that causes death at an early stage in development; a recessive lethal allele kills individuals that are homozygous for the allele; a dominant lethal allele kills both heterozygotes and homozygotes

29
Q

Genomic imprinting

A

differential expression of a gene depending on whether it is inherited from the male or female parent

30
Q

Anticipation

A

phenomenon in which a genetic trait becomes more strongly expressed, or is expressed at an earlier age, as it is passed from generation to generation

31
Q

Hemizygous

A

possession of a single allele at a locus; males of organisms with XX-XY sex determination are hemizygous for X-linked loci because their cells possess a single X chromosome

32
Q

Consanguinity

A

mating between closely related people

33
Q

Monoecious

A

refers to an individual organism that has both male and female reproductive structures

34
Q

Dioecious

A

belonging to a species in which an individual organism has either male or female reproductive structures