TERMS FOR UNIT 2 Flashcards

1
Q

What are the 3 main events of Meiosis I?

A

prophase I: homologous pair undergoes synapsis & crossing over between non sister chromatids with subsequent appearance of chiasmata

metaphase I: chromosomes line up as homologous pairs on metaphase plate

anaphase I: homologues seperate from each other, sister chromatids remain joined @ centromere

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2
Q

synapsis

A

The pairing of replicated homologous chromosomes during prophase I of meiosis.

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3
Q

crossing over

A

The reciprocal exchange of genetic material between nonsister chromatids during prophase I of meiosis.

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4
Q

tetrad

A

A paired set of homologous chromosomes, each composed of two sister chromatids. Form during prophase I of meiosis.

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5
Q

chiasma

A

An X-shaped region in each tetrad; represents homologous chromatids that have exchanged genetic material through crossing over during meiosis.

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6
Q

complete dominance of 1 allele

A

Heterozygous phenotype
same as that of homozygous dominant

PP or Pp

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7
Q

incomplete dominance of either allele

A

Heterozygous phenotype
intermediate between the
two homozygous phenotypes

C^R C^R, C^R C^W, or C^W C^W

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8
Q

codominace

A

Both phenotypes
expressed in heterozygotes

I^A I^B

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9
Q

multiple alleles

A

In the population, some
genes have more than two
alleles

I^A, I^B, i

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10
Q

Epistasis

A

The phenotypic expression
of one gene affects the
expression of another gene

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11
Q

helicase

A

unwinds parental double helix @ replication forks

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12
Q

single-strand binding protein

A

binds to and stabilizes single-stranded DNA until it is used as a template

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13
Q

topoisomerase

A

relieves overwinding strain ahead of replication forks by breaking, swivelling and rejoining DNA strands

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14
Q

primase

A

synthesizes RNA primer at 5’ end of leading strand and 3’ end of each Okazaki fragment of lagging strand

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15
Q

DNA pol III

A

Using parental DNA as a template, synthesizes new DNA strand by adding nucleotides to an RNA primer or a preexisting DNA strand

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16
Q

DNA pol I

A

Removes RNA nucleotides of primer from 5’ end and replaces them with DNA nucleotides

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17
Q

DNA ligase

A

Joins Okazaki fragments of lagging strand; on leading strand, joins 3’ end of DNA that replaces primer to rest
of leading strand DNA

18
Q

messenger RNA - mRNA

A

Carries information specifying amino acid sequences of proteins from DNA to ribosomes

19
Q

transfer RNA - tRNA

A

Serves as translator molecule in protein synthesis; translates mRNA codons into amino-acids

20
Q

ribosomal RNA - rRNA

A

Plays catalytic (ribozyme) roles and structural roles in ribosomes

21
Q

primary transcript

A

Is a precursor to mRNA, rRNA, or tRNA, before being processed; some intron
RNA acts as a ribozyme, catalyzing its own splicing

22
Q

small nuclear RNA - sRNA

A

Plays structural and catalytic roles in spliceosomes, the complexes of protein and RNA that splice pre-mRNA

23
Q

chromosome

A

condensed complex of DNA & histone proteins

24
Q

sister chromosomes

A

while joined 2 sister chromatids make up one chromosome

25
exons & introns
coding regions for expressed DNA space holders, eventually get spliced out
26
homozygous vs heterozygous
having 2 identical alleles for gene having 2 different alleles for gene
27
note lecture 6
28
Explain Griffith's experiments: rat & bacteria strains
- s strain (smooth, capable of infection), r strain (rough) - S cells into mouse it dies - R cells into mouse it lives - heated S cells so they couldn't cause infection - mixed heated S cells & R cells into mouse but it died - transformation caused by DNA
29
Bacteriophages & radioactive phosphorus & sulfur experiments
- DNA contains phosphorus but no sulfur. - Protein contains sulfur but no phosphorus. - Both sulfur and phosphorus have radioisotopes (355, 32P) - If only DNA is radioactively labelled, then when you detect radioactivity you can conclude that it is coming from DNA. - protein was only on outer coating - DNA being injected into cell by bacteriophages
30
Structure of DNA - Xray
- Helical structure - Sugar-phosphate backbone on the outside - Uniform width of 2 nm
31
Chargaff's rules
% of A & T equivalent % of C & G equivalent
32
Double helix model
- 2 antiparallel strands held together by hydrogen bonding between bases - base pairing - DNA uses semiconservative model to replicate
33
RNA polymerase in transcription
RNA polymerase attaches to DNA, makes sure the free nucleotide bases match up in complementary way w/ bases on the template strand of DNA (ensures they are lined up, attacted and assembled) then RNA transcript can let them leave nucleus
34
Ribosome role in translation
- ribosome (organizes translation) - attaches to mRNA transcript - reads it and brings in amino acids by tRNAs that have anticodon tag at one and that matches up w/ codons on RNA transcript & at other and there is an amino acid. - ribosome attaches all these amino acids together
35
Overview of transcription
- strands of DNA separate along a stretch of the molecule - free bases attach to corresponding bases on template strand to make mRNA - newly formed mRNA moves into the cytoplasm (eukaryotes; already in cytoplasm in prokaryotes)
36
Overview of translation
- ribosome moves along the stand of mRNA three bases at a time - ribosome brings specific amino acids into place according to the sequence of bases in the mRNA triplets - at end of the mRNA strand ribosome detaches from the assembled chain of amino acids - chain folds / subunits combine form the newly completed protein
37
trp operon overview
- The trp operon is expressed (turned "on") when tryptophan levels are low and repressed (turned "off") when they are high. - The trp operon is regulated by the trp repressor. - repressible operon (tryptophan binds and prevents RNA polymerase from reading)
38
lac operon overview
- Lac operon contains genes involved in metabolism. - The genes are expressed only when lactose is present and glucose is absent. - The operon is turned on and off in response to the glucose and lactose levels: catabolite activator protein and lac repressor. - inducible operon
39
restriction enzymes
- Enzymes, naturally present in bacteria, protect against vial infection - "Cut" DNA at sequence- specific sites
40
gene cloning (define plasmid too)
plasmid - circular DNA present in bacteria, used to move genes into it applications: - Antibiotic production move genes into bacteria - Synthesis of human proteins for therapeutic use ex.: clotting factors, insulin) - pesticide-resistant crops
41
PCR
- Make thousands of copies of a piece of DNA - Check for the presence of a sequence of interest - Used to verify species - Identify illegal import/export/food products - "DNA-barcoding"
42
DNA sequencing
- Human genome project - Many subsequent full genomes have been sequenced - Purpose: to find & characterize genes with deleterious phenotypes