Unit 3 List 2 DNA & Heredity Flashcards

1
Q

allele

A

one of two or more alternative forms of a gene that arise by mutation and are found at the same place on a chromosome.

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2
Q

centromere

A

the region of a chromosome to which the microtubules of the spindle attach, via the kinetochore, during cell division.

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3
Q

chromatid

A

each of the two threadlike strands into which a chromosome divides longitudinally during cell division. Each contains a double helix of DNA.

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4
Q

Chromosome

A

a threadlike structure of nucleic acids and protein found in the nucleus of most living cells, carrying genetic information in the form of genes.

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5
Q

codon (chart)

A

a chart of all the codons and the amino acids they stand for

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6
Q

crossing over

A

a cellular process that happens during meiosis when chromosomes of the same type are lined up

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7
Q

daughter cell

A

the cells that are formed after cell division

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8
Q

deletion

A

A type of genetic change that involves the absence of a segment of DNA

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9
Q

diploid

A

the presence of two complete sets of chromosomes in an organism’s cells, with each parent contributing a chromosome to each pair

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10
Q

DNA

A

the molecule that carries genetic information for the development and functioning of an organism

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11
Q

fertilization

A

the union of two gametes. During fertilization, sperm and egg fuse to form a diploid zygote to initiate prenatal development

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12
Q

frameshift

A

a genetic mutation caused by a deletion or insertion in a DNA sequence that shifts the way the sequence is read

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13
Q

gamete

A

a reproductive cell of an animal or plant

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14
Q

gene

A

The basic unit of heredity passed from parent to child

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15
Q

gene mutation

A

a change to a gene’s DNA sequence to produce something different. It creates a permanent change to that gene’s DNA sequence

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16
Q

genetic code

A

a set of three-letter combinations of nucleotides called codons, each of which corresponds to a specific amino acid or stop signal

17
Q

genetic variation

A

a term used to describe the variation in the DNA sequence in each of our genomes

18
Q

haploid

A

a cell that contains a single set of chromosomes

19
Q

homologous chromosome

A

pairs of chromosomes in a diploid organism that have similar genes, although not necessarily identical

20
Q

independent assortment

A

a genetic principle that states that the alleles of two genes will segregate into daughter cells independent of one another

21
Q

insertion

A

a type of mutation that involves the addition of one or more nucleotides into a segment of DNA

22
Q

meiosis

A

a type of cell division that reduces the number of chromosomes in the parent cell by half and produces four gamete cells

23
Q

meiosis I

A

a specialized type of cell division that reduces the chromosome number by half, resulting in the production of four genetically distinct haploid cells from an original diploid cell

24
Q

meiosis II

A

a mitotic division of each of the haploid cells produced in meiosis I

25
monosomy
the absence of one member of a pair of chromosomes
26
mutagen
a chemical or physical agent capable of inducing changes in DNA called mutations
27
mutation
a change in a DNA sequence. Mutations can result from DNA copying mistakes
28
nondisjunction
he failure of the chromosomes to separate, which produces daughter cells with abnormal numbers of chromosomes
29
offspring
the young creation of living organisms, produced either by sexual or asexual reproduction
30
parent cell
A cell that is the source of other cells
31
point mutation
A genetic alteration caused by the substitution of a single nucleotide for another nucleotide
32
replication
the process by which the genome's DNA is copied in cells.
33
sexual reproduction
the production of new organisms by the combination of genetic information of two individuals of different sexes
34
somatic cell
the cells in the body other than sperm and egg cells
35
substitution
a type of mutation in which one nucleotide is replaced by a different nucleotide
36
trisomy
The presence of an extra chromosome in some or all of the body's cells.
37
trait
specific characteristic of an individual