Unit 3 List 2 DNA & Heredity KYS Flashcards

1
Q

allele

A

One of two or more versions of a genetic sequence at a particular region on a chromosome

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2
Q

centromere

A

structure in a chromosome that holds together the two chromatids

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3
Q

chromatid

A

one of the two identical halves of a chromosome that has been replicated in preparation for cell division

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4
Q

chromosome

A

A structure found inside the nucleus of a cell; made up of proteins and DNA

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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 mutation that involves the loss of one or more nucleotides from 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

a molecule that carries genetic information for an organism

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11
Q

fertilization

A

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

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12
Q

frameshift

A

An insertion or deletion involving a number of base pairs that is not a multiple of three, which consequently disrupts the triplet reading frame of a DNA sequence

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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

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16
Q

genetic code

A

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

17
Q

genetic variation

A

a measure of the genetic differences that exist within a population

18
Q

haploid

A

the presence of a single set of chromosomes in an organism’s cells

19
Q

homologous chromosome

A

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

20
Q

insertion

A

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

20
Q

independent assortment

A

the alleles of two (or more) different genes get sorted into gametes independently of one another

21
Q

meiosis

A

a process where a single cell divides twice to produce four cells containing half the original amount of genetic information

22
Q

meiosis I

A

the number of cells is doubled but the number of chromosomes is not

23
Q

meiosis II

A

the second division in meiosis in which chromatids of each chromosome are segregated equally into daughter cells

24
monosomy
the condition in which only one chromosome from a pair is present in cells rather than the two copies usually found in diploid cells
25
mutagen
a chemical or physical agent capable of inducing changes in DNA called mutations
26
mutation
Any change in the DNA sequence of a cell
27
nondisjunction
the failure of the chromosomes to separate, which produces daughter cells with abnormal numbers of chromosomes
28
offspring
the young creation of living organisms, produced either by sexual or asexual reproduction
29
parent cell
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
30
point mutation
change within a gene in which one base pair in the DNA sequence is altered
31
replication
the process by which the genome's DNA is copied in cells
32
sexual reproduction
the production of new organisms by the combination of genetic information of two individuals of different sexes
33
somatic cell
the cells in the body other than sperm and egg cells
34
substitution
a type of mutation in which one nucleotide is replaced by a different nucleotide
35
trisomy
The presence of an extra chromosome in some or all of the body's cells
36
trait
a specific characteristic of an individual