Unit 3 List 2 DNA & Heredity GLW 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

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

threadlike structures made of protein and a single molecule of DNA that serve to carry the genomic information from cell to cell

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5
Q

codon

A

A codon is a trinucleotide sequence of DNA or RNA that corresponds to a specific amino acid.

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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

the removal or obliteration of written or printed matter, especially by drawing a line through it.

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9
Q

diploid

A

(of a cell or nucleus) containing two complete sets of chromosomes, one from each parent.

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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

a complex multi-step process that is complete in 24 hours.

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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 mature haploid male or female germ cell which is able to unite with another of the opposite sex in sexual reproduction to form a zygote.

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14
Q

gene

A

(in informal use) a unit of heredity which is transferred from a parent to offspring and is held to determine some characteristic of the offspring.

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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

Genetic code refers to the instructions contained in a gene that tell a cell how to make a specific protein.

17
Q

genetic variation

A

Without genetic variation, some key mechanisms of evolutionary change like natural selection and genetic drift cannot operate.

18
Q

haploid

A

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

19
Q

homologous chromosome

A

made up of chromosome pairs of approximately the same length, centromere position, and staining pattern, for genes with the same corresponding loci

20
Q

independent assortment

A

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

21
Q

insertion

A

the action of inserting something.

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

24
Q

meiosis II

A

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

25
Q

monosomy

A

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
Q

mutagen

A

Anything that causes a mutation (a change in the DNA of a cell)

27
Q

mutation

A

Any change in the DNA sequence of a cell.

28
Q

nondisjunction

A

a pair of homologous chromosomes has failed to separate or segregate at anaphase so that both chromosomes of the pair pass to the same daughter cell

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

occurs in a genome when a single base pair is added, deleted or changed

32
Q

replication

A

the action of copying or reproducing something.

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

cells in the body other than sperm and egg cells

35
Q

substitution

A

the action of replacing someone or something with another person or thing.

36
Q

trisomy

A

a chromosomal condition characterised by an additional chromosome

37
Q

trait

A

a distinguishing quality or characteristic, typically one belonging to a person.