Alberts, Ch 4 - DNA, Chromosomes and Genomes Flashcards

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1
Q

Base pair

A

Two nucleotides in an RNA or DNA molecule that are held together by hydrogen bonds, G-C, A-T/U

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2
Q

Centrosome

A

Centrally located organelle of animal cells that is the primary microtubule-organizing center (MTOC) and acts as the spindle pole during mitosis, usually in pairs called centrioles

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3
Q

Chromatin

A

Complex of DNAm, histones and non-histone proteins found in the nucleus of a eukaryotic cell, material of which chromosomes are made

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4
Q

Chromosome

A

Structure composed of a very long DNA molecule and associated proteins that carries part of the hereditary information of an organism, especially evident in cells undergoing mitosis

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5
Q

Complementary

A

Capable of forming a perfect base-paired duplex with each other, having biochemical or structural features that marry up so that noncovalent bonding is facilitated

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6
Q

Copy number variations (CNV)

A

A difference between two individuals in the same population in the number of copies of a particular block of DNA sequence, variation arises from occasional duplicaions and deletions of these sequences

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7
Q

Deoxyribonucleis acid (DNA)

A

Polynucletide formed from covalently linked deoxyribonucleotide units, store of hereditary information within a cell and carrier of information from generation to generation

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8
Q

Double helix

A

Three-dimensional structure of DNA, in which two antiparallel DNA chains held together by hydrogen-bonding wound into a helix

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9
Q

Epigenetic inheritance

A

Inheritance of phenotypicchanges in a cell or organism that do not result from changes in the nucleotide sequence of DNA, can be due to positive feedback loops of transcription regulators or heritable modifications in chromatin such as DNA methylation or histon modifications

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10
Q

Euchromatin

A

Region of interphase chromose that stains diffusely, “normal” chromatin as opposed to condensed heterochromatin

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11
Q

Exon

A

Segment of eukaryotic gene that consists of a sequence of nucleotides that will be represented in mRNA or in a final transfer, ribosomal or other mature RNA molecule, in protein-coding genes encode the amino acids in the protein

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12
Q

Gene

A

Region of DNA that is transcribed as a single unit and carries information for a discrete hereditary characteristic, usually corresponding to single protein or single RNA

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13
Q

Genome

A

Totality of genetic information belonging to a cell or an organism, the DNA that carries the information

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14
Q

Heterochromatin

A

Chromatin that is highly condensed even in interphase, generally transcriptionally inactive

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15
Q

Histone

A

One of a group of small abundant proteins, rich in arginine and lysine, that combine to form nucleosome coresaround which DNA is wrapped

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16
Q

Histone H1

A

Linker histone protein that binds to DNA where it exits from a nucleosome and helps package nucleosomes ino the 30-nmchromatin fiber

17
Q

Homolog

A

Oneof two or more genes that are similar in sequence as a result of derivation from the same ancestral gene, covers both orthologs and paralogs

18
Q

Homologous

A

Genes, proteins, or body structures that are similar as a reult of a shared evolutionary evolution

19
Q

Intron

A

Noncoding region of a eukaryotis gene that is transcribed into an RNA molecule but is then excised by RNA splicing during production of the mRNA or other functional RNA

20
Q

Karyotype

A

Display of the full set of chromosome that are arranged with respect to size, shape and number

21
Q

Lampbrush chromosome

A

Huge chromosome paired in preparation for meiosis, found in immature amphibian eggs

22
Q

Mitotic chromosome

A

Highly condensed duplicated chromosome as seen at mitosis, consisting oftwo sister chromatids held together at the centromere

23
Q

Nucleosome

A

Beadlike structure in eukaryotic chromatin, composed of a short length of DNA wrapped around an octameric core oh histone proteins, fundamental structure unit of chromatin

24
Q

Position effect variegation

A

Alteration in gene expression resulting from change in the position of gene in relation to other chromosomal domains, especially heterochromatic domains, when an active gene is placed next to heterochromatin, inactivating influence of heterochromatin can spread to affect the gene to a variable degree

25
Q

Pseudogene

A

Nucleotide sequence. Of DNAthat has accumulated multiple mutations thathave rendered an ancestral gene inactive and nonfuntional

26
Q

Purifying selection

A

Natural selection operating in a population to slow genome changes and reduce divergence by eliminating individuals carrying deleterious mutations

27
Q

Replication origin

A

Location on a DNA molecule at which duplication of DNA begins

28
Q

Single-nucleotide polymorphism (SNP)

A

Variation between individuals in a population due to a relatively common difference in a specific nucleotide at a defined point in the DNA sequence

29
Q

Telomere

A

End of a chromosome, associated with a characteristic DNA sequence that is replicated in a special way, counteracts tendency of chromosome otherwise to shorten with each round of replication

30
Q

Template

A

Single strand of DNA or RNA whose nucleotide sequence acts as a guid for synthesis of a complementary strand

31
Q

Antiparallel

A

Describesthe relative orientation of the two strands in a DNA double helix or two paired regions of a polypeptide chain, polarity of oone strand is opposite from the other

32
Q

Centromere

A

Constricted region of a mitotic chromosome that holds sister chromatids together, also the site on DNA where kinetochore forms so as to capture microtubules from mitotic spindle