Unit 3 List 2 DNA & Heredity AKT Flashcards

1
Q

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

A

allele

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1
Q

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

A

centromere

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2
Q

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

A

chromatid

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3
Q

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

A

chromosome

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4
Q

A table can be used to translate a genetic code into a sequence of amino acids.

A

codon chart

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5
Q

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

A

crossing over

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6
Q

the cells that are formed after cell division

A

daughter cell

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7
Q

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

A

deletion

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8
Q

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

A

diploid

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9
Q

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

A

DNA

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10
Q

The process by which two gametes (reproductive cells having a single, haploid set of chromosomes) fuse to become a zygote, which develops into a new organism

A

fertilization

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11
Q

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

A

frameshift

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12
Q

a reproductive cell of an animal or plant

A

gamete

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13
Q

The basic unit of heredity passed from parent to child

A

gene

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14
Q

a change to a gene’s DNA sequence to produce something different

A

gene mutation

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15
Q

the instructions contained in a gene that tell a cell how to make a specific protein

A

genetic code

16
Q

the difference in DNA among individuals or the differences between populations among the same species

A

genetic variation

17
Q

a cell that contains a single set of chromosomes

18
Q

a set of one maternal and one paternal chromosome that pair up with each other inside a cell during fertilization

A

homologous chromosome

19
Q

describes how different genes independently separate from one another when reproductive cells develop

A

independent assortment

20
Q

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

21
Q

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

22
Q

a type of cell division unique to germ cells

23
Q

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

A

meiosis II

24
the absence of one member of a pair of chromosomes
monosomy
25
a chemical or physical agent capable of inducing changes in DNA called mutations
mutagen
26
an alteration in the nucleic acid sequence of the genome of an organism, virus, or extrachromosomal DNA
mutation
27
the failure of the chromosomes to separate, which produces daughter cells with abnormal numbers of chromosomes
nondisjunction
28
the young creation of living organisms, produced either by sexual or asexual reproduction
offspring
29
A cell that is the source of other cells, as a cell that divides to produce two or more daughter cells, or a stem cell that is a progenitor of other cells or is the first in a line of developing cells
parent cell
30
A genetic alteration caused by the substitution of a single nucleotide for another nucleotide
point mutation
31
the process by which a double-stranded DNA molecule is copied to produce two identical DNA molecule
replication
32
the production of new organisms by the combination of genetic information of two individuals of different sexes
sexual reproduction
33
the cells in the body other than sperm and egg cells
somatic cell
34
a type of mutation in which one nucleotide is replaced by a different nucleotide
substitution
35
The presence of an extra chromosome in some or all of the body's cells
trisomy
36
a specific characteristic of an individual
trait