Unit 3 List 2 DNA & Heredity Flashcards

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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
Q

monosomy

A

the absence of one member of a pair of chromosomes

26
Q

mutagen

A

a chemical or physical agent capable of inducing changes in DNA called mutations

27
Q

mutation

A

a change in a DNA sequence. Mutations can result from DNA copying mistakes

28
Q

nondisjunction

A

he failure of the chromosomes to separate, which produces daughter cells with abnormal numbers of chromosomes

29
Q

offspring

A

the young creation of living organisms, produced either by sexual or asexual reproduction

30
Q

parent cell

A

A cell that is the source of other cells

31
Q

point mutation

A

A genetic alteration caused by the substitution of a single nucleotide for another nucleotide

32
Q

replication

A

the process by which the genome’s DNA is copied in cells.

33
Q

sexual reproduction

A

the production of new organisms by the combination of genetic information of two individuals of different sexes

34
Q

somatic cell

A

the cells in the body other than sperm and egg cells

35
Q

substitution

A

a type of mutation in which one nucleotide is replaced by a different nucleotide

36
Q

trisomy

A

The presence of an extra chromosome in some or all of the body’s cells.

37
Q

trait

A

specific characteristic of an individual