Chater 8 Flashcards

(41 cards)

1
Q

Double helix DNA molecule winds around protein called

A

Histones

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2
Q

Histones

A

(H1, H2a,H2 , H3, H4)

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3
Q

Eight of these histones group together to form a unit called

A

Nucleosome

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4
Q

These nucleosome then wind in a helical fashion to form a coil called

A

Selenoid

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5
Q

The coil wraps even further to form

A

Supercoils

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6
Q

These supercoils form a fiber of DNA- protein called

A

Chromatin

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7
Q

these chromatins condenses even further called

A

Chromosome

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8
Q

detects the placement of nucleosomes

A

NUCLEASes

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9
Q

enzymes that cut the double helix in the linker
region (the part of the double helix that is exposed
between histones)

A

Nucleases

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10
Q

associated with histone HI

A

30- micron- fiber

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11
Q

first classic indicator of apoptosis

A

30- micron- fiber

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12
Q

state of the compaction of the DNA double heliX

A

CHROMOSOME TOPOLOGY

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13
Q

Closed Chromatin

A

Heterochromatin:

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14
Q

open chromatin

A

Euchromatin

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15
Q

distinguisned historically by their relative size
and centromere placement.

A

CHROMOSOME MORPHOLOGY

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16
Q

distinguisned historically by their relative size
and centromere placement.

A

CENTROMERE

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17
Q

is the site of attachment of the chromosome to the spindl apparatus.

18
Q

 the connection made between microtubules of the splindle and a protein complex.

19
Q

Long arm

20
Q

Short arm

21
Q

CYTOLOGICAL STAINS

A

Feurgen’s, wrights, Hematoxylin

22
Q

used to visualize chromosome.

A

Cytological stains

23
Q

can react with specific chromosome regions.

A

FLUORESCENT DYES and CHEMICAL DYES

24
Q

results in the formation of band patterns where
portions of the chromosome accept or reject the stain.

A

FLuORESCENT DYES and CHEMICAL DYES

25
stained with Fluorescent dyes such as Quinacrine and Quinacrine mustard
Q BANDING
26
gives an intense staining of the human y chromosome affects gene activity requires fluorescent microscope
Q banding
27
Stained with chemical due, Giemsa Stain
G banding
28
Mild treatment for G banding
2x standard saline citrate for 60 minutes at 68 c
29
To extract or denature proteins before Giemsa staining was found to map abbrerations and most commonly used staining method
Trypsin or orther Proteolytic agents
30
Feulgen staining after treatment w/ DNase I.
G banding
31
centromere Staining is ABSENT.
G banding
32
results from deletion of genetic regions from both ends of the chromosome and a joining of the ends to form ring.
RING CHROMOSOME
33
abnormal chromosome consisting of translocated or otherwise rearranged paris from two or more unidentified chromosomes pined to a normal chromosome.
DERIVATIVE CHROMOSOME
34
normal female karyotype
46,XX
35
Normal male karyotype
46,XY
36
results from extra chromosome 21
Down’s syndrome
37
caused by an extra X Chromosome in males (i.e. 47, xxy)
Klinefelters syndrome
38
widely used method to detect protein, RNA as well as DNA Structures in place in the cell or in situ.
INTERPHASE FISH
39
Growth of cells in culture is not required.
Interphase FISH
40
enhanced by the development of fluorescent probes that bind to metaphase chromosomol regions or to whole chromosomes
METAPHASE FISH
41
Probes that cover the entire chromosome or whole chromosome paints, are valueble for detecting small rearrangements that are not apparent by regular chromosome banding
METAPHASE FISH