Week 2 Flashcards

(35 cards)

1
Q

Model Species

A
Organism used to study biological phenomenon
Short life cycle
Cheap
Low junk DNA
Drosophila melanogaster
Escherichia coli
Arabidopsis thaliana
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2
Q

Bacteriophage

A

a virus that parasitizes a bacterium by infecting it and reproducing inside it

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3
Q

Blended inheritance

A

outdated theory that progeny inherits any characteristic as the average of the parents’ values of that characteristic

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4
Q

Gene

A

a sequence of nucleotides in DNA or RNA that encodes the synthesis of a gene product, either RNA or protein

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5
Q

Phenotype

A

composite observable characteristics or traits of an organism

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6
Q

Alleles

A

one of two or more versions of a gene. An individual inherits two alleles for each gene, one from each parent

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7
Q

Gametes sex cells

A

organism’s reproductive cells
haploid cells, and each cell carries only one copy of each chromosome
egg or sperm

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8
Q

Linkage group

A

all of the genes on a single chromosome. They are inherited as a group; that is, during cell division they act and move as a unit rather than independently

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9
Q

Chromosome

A

a DNA molecule with part or all of the genetic material of an organism

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10
Q

Genome

A

genetic material of an organism

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11
Q

Dominant

A

one variant of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome

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12
Q

Recessive

A

masked or overriden variant of a gene

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13
Q

Genotype

A

an organism’s complete set of heritable genes, or genes that can be passed down from parents to offspring

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14
Q

Co-dominant

A

neither allele is recessive and the phenotypes of both alleles are expressed

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15
Q

Partial dominance

A

production of an intermediate phenotype in individuals that are heterozygous for the gene concerned (i.e. the heterozygote shares a phenotype that is quantitatively intermediate between those of the corresponding homozygotes)

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16
Q

Punnett squares

A

a square diagram that is used to predict the genotypes of a particular cross or breeding experiment

17
Q

Genotype ratio

A

the number of times a genotype would appear in the offspring after a test cross

18
Q

Phenotype ratio

A

the relative number of offspring manifesting a particular trait or combination of traits

19
Q

Pedigree chart

A

a diagram that shows the occurrence and appearance of phenotypes of a particular gene or organism and its ancestors from one generation to the next

20
Q

Homozygotes

A

an individual having two identical alleles of a particular gene or genes and so breeding true for the corresponding characteristic

21
Q

Heterozygotes

A

an individual having two different alleles of a particular gene or genes, and so giving rise to varying offspring

22
Q

Somatic Cells

A

any cell of the body except sperm and egg cells
diploid
mutations can affect the individual but will not be passed down

23
Q

Mitosis

A

part of the cell cycle when replicated chromosomes are separated into two new nuclei
gives rise to genetically identical cells in which the number of chromosomes is maintained

24
Q

Meiosis

A

special type of cell division in sexually-reproducing organisms used to produce the gametes, such as sperm or egg cells
two rounds of division that ultimately result in four cells with only one copy of each chromosome

25
Recombination
exchange of genetic material between different organisms which leads to production of offspring with combinations of traits that differ from those found in either parent
26
Haploid
having the number of sets of chromosomes normally found in a gamete having exactly half the number of sets of chromosomes found in a somatic cell
27
Diploid
cells have two homologous copies of each chromosome
28
Triploid
3 sets of chromosomes
29
Tetraploid
4 sets of chromosomes
30
Polyploid
state where all cells have multiple sets of chromosomes beyond the basic set, usually 3 or more
31
Aneuploidy
state where one or more individual chromosomes of a normal set are absent or present in more than their usual number of copies Down's syndrome
32
Trisomy
a type of polysomy in which there are three instances of a particular chromosome, instead of the normal two. A trisomy is a type of aneuploidy
33
Nondisjunction
failure of homologous chromosomes or sister chromatids to separate properly during cell division.
34
Karotype
process by which photographs of chromosomes are taken in order to determine the chromosome complement of an individual, including the number of chromosomes and any abnormalities
35
Sex-linked genes
a trait in which a gene is located on a sex chromosome. In humans, the term generally refers to traits that are influenced by genes on the X chromosome. This is because the X chromosome is large and contains many more genes than the smaller Y chromosome