Chapter 16 Flashcards

(43 cards)

1
Q

What did Morgan experiment show

A

-Th Morgan group showed that gene exist as part of chromosomes, the two chemical components of chromosomes-DNA and protein emerged as leading candidates of genetic material.

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2
Q

Transformation

A

Defined as a change in genotype and phenotype due to the assimilation of external DNA by a cell. American Maclyn MaCarry and Canadian Colin Macloed identified the transforming substance as DNA

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3
Q

Bacteriophage

A

Meaning bacteria-enter

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4
Q

Virus

A

A protein coat which has DNA inside, to produce more viruses, a virus must infect a cell and take over its metabolic machinery

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5
Q

What did Hershey and chase discover?

A

Hershey and chase found that phage DNA enter the host call but the phage protein did not. This result further showed that the DNA inside the cell played an ongoing role during infection process. Also concluded that DNA injected had genetic information that cell produce new virals.

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6
Q

What does DNA consist of ?

A
  • a nitrogenous base containing adenine,thymine,guanine and cytosine
  • a pentode sugar called deoxyribose
  • phosphate group
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7
Q

Complementary base pairing

A

DNA base are complementary A binds to T and G bind to C. The number of A is equal to the number of T, and the number of g is equal c.

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8
Q

Chargoff rule

A

(1) DNA base composition varies between species,

(2) for each species, the percentages of A and T bases are roughly equal, as are those of G and C bases.

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9
Q

Franklin discovery

A

-Franklin discovered double helix model. Her model was appealing because it put the negative charged phosphate group facing the surrounding while relatively hydrophobic nitrogenous bases were hidden in the interior .

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10
Q

Antiparallel

A

Two sugar phosphate backbone are antiparallel- there subunit move in opposite direction constructing a ladder or rope like structure

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11
Q

Purine vs pyrimidines

A

Adenine and guanine are purine (pure as gold)

Cytosine and thymine are pyrimidine

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12
Q

No hydrogen bond between bases

A
  • adenine can for for two hydrogen bonds with thymine

- guanine for, three hydrogen bonds with cytosine

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13
Q

What did Meselson-Stahi experiment showed ?

A

Showed that DNA replication is semi conservative= the parental molecules unwind,and each strand then serves as a template for the synthesis of a new strand according to base-pairing rule

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14
Q

Origin of replication

A

-the replication of chromosomal DNA begins at particular sites is called origin of replication. Protein recognises a DNA sequence and starts the process. This origin forms a double in strand prior to replication

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15
Q

Primer

A

The RNA chain

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16
Q

Primase

A

The enzyme used to synthesis RNA chain

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17
Q

Stages of DNaA replication

A

1) helically unwind the parental double helix
2)molecules of single strand binding protein stabilise the unfounded template
3) the easing strand is continuously synthesised in 5’ to 3’ direction by DNA polymerase 3
4)primase begin synthesis of the RNA primer on Okazaki fragment (lagging strand)
5) DNA pol 3 Is complete synthesis of fragment 4. When it reaches the RNA primer of fragment 3, it will detach and begin adding DNA nucleotide to the 3’ end of the fragment 5 primer in the replication fork.
6) DNA pol I removes the primer from the 5¿ end of fragment 2, replacing it with DNA nucleotides added one by one to the 3’ end of fragment 3. After the last addition, the backbone is left with
a free 3’
7)DNA ligand joins the fragment 3’dnd of fragment 2 to the 5’ end of fragment 1

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18
Q

Leading strand

A

Continuous strand

19
Q

Lagging strand

A

Non continuous strand

20
Q

Okazaki fragment

A

The segment of lagging stand

21
Q

Helicase

A

An enzymes that unwinds the DNA strand at replication fork

22
Q

Sing.e strand binding protein

A

Protein that binds to unpaired DNA strands

23
Q

Topoisomerase

A

An enzyme that help relieve this strain by breaking, swivelling and rejoining DNA strand,

24
Q

Protein involved in initial replication

A
  • topoisomerase break, swivels and rejoin parental DNA ahead of the replication fork, reliving the strain to unwind the.
  • primase synthesis RNA primer uses ping the parental DNA as template
  • helicase unwinds and separates the parental DNA strands
  • single strand binding protein stabilise the unfounded parental strand
25
Direction of leading vs lagging
Leading 5’-3’ | Lagging 5’-3’
26
DNA pol 1 vs 3
Pol 3- attaches nucleotide | Pol1 - replaces RNA with DNA
27
DNA ligaments
Join okazaki fragment of lagging strand
28
Mismatch in strand
-DNA polymerase proofreads each nucleotide against its template as soon as its covalently bounded to growing strand, upon finding incorrect paired nucleotide, the polymerase removes it and resume synthesis
29
Mismatch repair
Other enzymes remove and replace incorrectly paired nucleotidethat have resulted from replication error .
30
Nuclease
An enzyme that removes damage
31
Nucleotide excision
DNA repair system
32
Stages of nucleotide excision
- teams of enzyme detect and repair damages DNA, such as thymine dimmer which distort DNA molecules - a nuclease enzyme cut the damaged DNA strand at two points, and the damaged section is removed. - Repair synthesis by a DNA polymerase fills in the missing nucleotides. - DNA ligase seals the free end of the new DNA to the old DNA, making the strand complete.
33
Mutation
A permanent change in DNA sequence
34
Shortening at the end of linear molecules
Primer removed cannot replaced with DNA beacause no 3 end available for DNA polymerase
35
Telomerase
DNA molecules have special nucleotide sequence, these sequence do not have gene and are subsequently lost during replication. As a result aging occurs Function - telomeric DNA prevent the staggered end of the daughter molecules from activating cell system to monitor DNA damage - protect against gene shortening
36
Telomerase
Enzyme that catalysis the lengthening of telomeres in eukaryotic germ cell this restoring their original length. Is not activated in most somatic cell.
37
Nucleoid
A dense non bounded region of DNA In Bacterium
38
His tones
Protein that are responsible for the first level of DNA packing in chromatin. Four types of his tones are most common H2A,H2B, H3 and H4
39
Nucleoside
The basic unit of DNA packing;the string between heads is called linker
40
Chromatin
Protein that fits into nucleus through an elaborating multilevel packaging
41
Heterochromatin
More compact than eucropatin | -inaccessible to the machinery in the cell responsible for transcribing nahe genetic coded in the DNA
42
Euchromatin
- less compact more diverse than heterochromatin | - DNA accessible to this machinery so the gene presented in euchromatin can be transcribed.
43
Nucleosomes
The histones bond to each other th the DNA to form nucleosomes