Chater 8 Flashcards

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.

A

CENTROMERE

18
Q

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

A

KINETOCHORE

19
Q

Long arm

A

q

20
Q

Short arm

A

p

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
Q

stained with Fluorescent dyes such as Quinacrine and Quinacrine mustard

A

Q BANDING

26
Q

gives an intense staining of the human y chromosome
affects gene activity requires fluorescent microscope

A

Q banding

27
Q

Stained with chemical due, Giemsa Stain

A

G banding

28
Q

Mild treatment for G banding

A

2x standard saline citrate for 60 minutes at 68 c

29
Q

To extract or denature proteins before Giemsa staining was found to map abbrerations and most commonly used staining method

A

Trypsin or orther Proteolytic agents

30
Q

Feulgen staining after treatment w/ DNase I.

A

G banding

31
Q

centromere Staining is ABSENT.

A

G banding

32
Q

results from deletion of genetic regions from both ends of the chromosome and a joining of the ends to form
ring.

A

RING CHROMOSOME

33
Q

abnormal chromosome consisting of translocated or otherwise rearranged paris from two or more
unidentified chromosomes pined to a normal
chromosome.

A

DERIVATIVE CHROMOSOME

34
Q

normal female karyotype

A

46,XX

35
Q

Normal male karyotype

A

46,XY

36
Q

results from extra chromosome 21

A

Down’s syndrome

37
Q

caused by an extra X Chromosome in males (i.e.
47, xxy)

A

Klinefelters syndrome

38
Q

widely used method to detect protein, RNA as well as DNA Structures in place in the cell or in situ.

A

INTERPHASE FISH

39
Q

Growth of cells in culture is not required.

A

Interphase FISH

40
Q

enhanced by the development of fluorescent probes that bind to metaphase chromosomol regions or to whole chromosomes

A

METAPHASE FISH

41
Q

Probes that cover the entire chromosome or
whole chromosome paints, are valueble for
detecting small rearrangements that are not
apparent by regular chromosome banding

A

METAPHASE FISH