Genetics And Biotechnology Flashcards

0
Q

Inactive densely packed chromatin during INTERPHASE

A

Heterochromatin

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1
Q

Total amount of purine = amount of pyrimidine

A

Chargaffs rule

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2
Q

Active, lightly stained chromatin

A

Euchromatin

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3
Q

Histones are high in 2 types of amino acids

A

Arginine and lysine

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4
Q

Phase of cell cycle: DNA replication

A

S phase

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5
Q

Protein that recognize origin of replication

A

DNA A protein

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6
Q

Unwinds the double helix

A

Helicase

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7
Q

Maintains separation of parental strands

A

Single stranded DNA binding protein

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8
Q

Remove supercoils

A

Tropoisomerase

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9
Q

Cleaves both strand of supercoils

Target of quinolones

A

Gyrase

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10
Q

Synthesize RNA (Primers)

A

Primase

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11
Q

Catalyze chain elongation and proofreads

A

Polymerase 3

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12
Q

Removes RNA primers

A

Polymerase 1

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13
Q

Fills in gaps

A

Polymerase 1

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14
Q

Seals in nicks between okazaki fragments

A

Ligase

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15
Q

Enzyme found in HIV/ retroviruses

A

Reverse transcriptase

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16
Q

Production of thymine dimers due to exposure to UV light

A

Xeroderma pigmentosa

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17
Q

Start codon

A

AUG

18
Q

Antibiotic that binds to the 30s subunit

A

Stremtomycin

19
Q

Antibiotic that binds to the 50s subunit

A

Clindamycin and erythromycin

20
Q

Antibiotic that inhibits peptidyltransferase

A

Chloramphenicol

21
Q

Antibiotic that Binds tob subunit of bacterial DNA dependent RNA polymerase

A

Rifampicib

22
Q

Toxin that inactivates eEf-2

A

Diphtheria toxin

23
Q

Any heritable change in the DNA base sequence

A

Mutation

24
Q

Point mutation of purine-pyrimidine to purine-pyrimidine

A

Transition

25
Q

Point mutation of purine-pyrimidine to pyrimidine-purine

A

Transversion

26
Q

Change in 3rd position of codon that code for same amino acid

A

Silent mutation

27
Q

New codon is a stop codon

A

Nonsense

28
Q

New codon is a different amino acid

A

Missense

29
Q

Deletion or addition of a base

A

Frameshift mutation

30
Q

3 diseases associated with splice donor or acceptor

A

Tay sachs
Gaucher
B-thalassemia

31
Q

Triple repeat expansion: CAG

A

Huntington

32
Q

Triple repeat expansion: CCG

A

Fragile X syndrome

33
Q

Triple repeat expansion: CDG

A

Myotonic dystrophy

34
Q

Used to deduce original sequence of DNA

A

Sanger DNA sequencing

35
Q

Used to synthesize many copies of desired fragment of DNA

A

PCR

36
Q

Used to determine which restriction fragment of DNA are associated with a particular gene.
A DNA sample is is placed on a gel

A

Southern blot

37
Q

Involves radioactive DNA probe binding to sample RNA

A

Northern blot

38
Q

Measure amount of antigen or antibody

A

Western blot

39
Q

Nucleic acid sequences are arranged in grids on glass or silicon

A

Microarrays

40
Q

Biothechnology used in localization of genes and direct visualization of anomalies at molecular level

A

FISH

41
Q

Diagnostic tool for diseases involving single- base changes or deletions/ insertions of DNA into a restriction fragment

A

Restriction fragment length polymorphism

42
Q

Production of recombinant DNA molecule that is self perpetuating

A

Cloning

43
Q

Treatment option for diseases caused by deficiency of a gene product

A

Gene therapy