Unit 3 List 2 DNA & Heredity 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

The region of the chromosome to which the spindle fiber is attached during cell division

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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

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5
Q

Codon (chart)

A

shows all of the possible three letter combinations of mRNA nucleotides, and for which amino acid each combination codes for

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6
Q

Crossing over

A

the exchange of genes between two chromosomes, resulting in non-identical chromatids that comprise the genetic material of gametes

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7
Q

Daughter cell

A

Either of the two cells formed when a cell undergoes cell division by mitosis

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8
Q

Depletion

A

The act or process of emptying, removal of a fluid, as the blood.

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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 process of combining the male gamete, or sperm, with the female gamete, or ovum

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12
Q

Frameshift

A

the insertion or deletion of nucleotide bases in numbers that are not multiples of three

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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 in one or more genes

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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

the presence of differences in sequences of genes between individual organisms of a species

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 originating from each parent. A cell would have two copies of chromosome 1 for example; one from the mother and one from the father.

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 in sexually reproducing organisms that reduces the number of chromosomes in gametes

23
Q

Meiosis I

A

The first of the two consecutive divisions of the nucleus of eukaryotic cell during meiosis, and composed of the following stages: prophase I, metaphase I, anaphase I, and telophase I.

24
Q

Meiosis II

A

the second division in meiosis in which chromatids of each chromosome are segregated equally into daughter cells. No DNA replication occurs during the interphase which precedes meiosis II.

25
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
26
Mutagen
a chemical or physical agent capable of inducing changes in DNA called mutations
27
Mutation
Any change in the DNA sequence of a cell. Mutations may be caused by mistakes during cell division, or they may be caused by exposure to DNA-damaging agents in the environment.
28
Nondisjunction
the failure of the chromosomes to separate, which produces daughter cells with abnormal numbers of chromosomes
28
Offspring
the product of the reproductive processes of a person, animal, or plant
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
a biological process of duplicating or producing an exact copy, such as a polynucleotide strand (DNA)
32
Sexual reproduction
occurs when the sperm from the male parent fertilizes an egg from the female parent, producing an offspring that is genetically different from both parents
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
34
Trisomy
The presence of an extra chromosome in some or all of the body's cells
34
Trait
a specific characteristic of an individual. Traits can be determined by genes, environmental factors or by a combination of both. Traits can be qualitative (such as eye color) or quantitative (such as height or blood pressure).