Chapter 3- Only Forgeting Cards Flashcards

(38 cards)

1
Q

Another word for chromosome

A

Coloured body given in 1880

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2
Q

When do sister chromatids separate?

A

Anaphase of mitosis

Anaphase II of meiosis

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3
Q

Cell cycle in order

A
G1
S phase
G2
Mitosis 
Cytokenesis
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4
Q

Linear DNA with 1 arm in ?

A

G1 phase
S phase
Anaphase of mitosis
Anaphase of meiosis

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5
Q

Describe chromosomes at interphase

A

Can be highly condensed and more extended because not all are paired up
Have v specific location

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6
Q

What is the constricted portion of each chromosome

A

Centromere

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7
Q

What is a constricted (central portion) of each chromosome

A

This section contains alpha satellite of nucleotide sequence of 171 repetitive

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8
Q

Centromere is always vondensed

A

Constitutive heterchromatin

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9
Q

Functions of centromere

A

Hold sisters
Bind to various proteins to facilitate cell division
Attach to kinetechors during M phase

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10
Q

Explain telomere region

A
Non coding regions of chromosome at the end
Short repeated sequence 
Include specialized proteins
Forms a capped end structure
Repeat TTAGGGTTAGGGTTAGGG
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11
Q

Function of telomeres

A

Binds with telomere binding proteins
Protect chromosome
Allow cells to distinguish chromosome ends from broken DNA
Prevent chromosome from fussing with one another
Attachment of DNA to nuclear scaffold

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12
Q

What happens when cell shortens and reach a critical point

A

Cellular seescense by apoptosis

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13
Q

What is a telomerase

A

An RNA containing enzyme (riboneucleo protein)
It adds more nucleotide to the 3’ end of telomere
Contain RNA components and enzyme

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14
Q

What is the function of RNA compartment in telomerase

A
  • template for synthesis of its DNA complement- reverse transcription
  • acts as a guide to attach to the telomere region
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15
Q

What is the function of enzyme compartment in telomerase

A

Catalyst

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16
Q

Where is telomerase present in

A
  • primordial germ cells
  • cancer cells
  • stem cells x although they do shorten over time
  • one celled organism
17
Q

Mutations in DNA can be spontaneous due to - - - —

18
Q

What causes mutations

A

Ionizing radiation
oxidative
Physical, chemical mitogen

19
Q

4 types of structure mutation

A

Duplication - double
Translocation - exchange btw non homologous , in meisois, occurs btw homologous
Inversion - flipped
Deletion

20
Q

Affects of translation

A
  • chromosome imbalance

- gene fussion activating harmless genes to oncogenes

21
Q

Human disease related to translation

A

Chronic myelogenic leukaemia

22
Q

Explain Chronic myelogenic leukaemia

A

Reciprocal translation btw 9 and 22 gene
C - ABL - BCR - fussion gene - Philadelphia
Leads to cont stimulation of WBC

23
Q

2 way translocation

24
Q

Ploidy of
Human ——- —
Mouse— — - -
Drosophila————

A

2n=46
2n=40
2n=80

25
How are karyotypes observed
Isolating mitotic cells and staining the chromosome
26
Karyotypes are also called
Painting bodies | Single stranded DNA tagged with fluorescence that hybridizes with DNA in chromosome therefore they will also light up
27
What lead to evolution , explain
Duplication | There is 98% similarities in non coding seq of humans and chimps
28
Mutation is number of chromosome is called
Non disjuntion
29
How does non - disjunction occur
When chromosomes fail to separate in meiosis I and II, gametes end up with more or less chromosome affecting the zygote
30
In 10,000, 800 chromosomally abnormal leads to 750 spontaneous miscarriage
31
If more then one chromosome duplicates, it leads to miscarriage
32
Down syndrome
Usually lethal other then 21 chromosome trisomy
33
Hay flick lucite
No. Of times a normal cell divides before cell division stops
34
What is the Chromosome difference btw humans and chimps
A fussion of no. 2 chromosomes in chimps | Humans have lot of duplications in non coding regions
35
If X and Y undergo non disjunction
Not fatal 3rd in inactive May be infertile
36
Tellings of karyotypes
Sex determination in human through presence or absence of Y chromosome No. Of chromosome in any given organism Chromosome aberration ( weather there are abnormal no. ) Structural mutations Cant detect Point mutation
37
Disorders associated with number mutations
1- Turner syndrome 45 chromosome instead of 46- lack X chromosome 2- kleinfelter syndrome 47 chromosome instead of 46 - gain X chromosome 3- Down syndrome Trisomy in chromosome number #21 Autosome 4- Edward syndrome Trisomy in chromosome number 18
38
Function of satellite DNA
Highly repetitive short DNA sequence | Ensure stability and protection of centromere region