Chapter 3- Only Forgeting Cards Flashcards

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 - - - —

A

Repressors

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

A

Reciprocal

24
Q

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

A

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

25
Q

How are karyotypes observed

A

Isolating mitotic cells and staining the chromosome

26
Q

Karyotypes are also called

A

Painting bodies

Single stranded DNA tagged with fluorescence that hybridizes with DNA in chromosome therefore they will also light up

27
Q

What lead to evolution , explain

A

Duplication

There is 98% similarities in non coding seq of humans and chimps

28
Q

Mutation is number of chromosome is called

A

Non disjuntion

29
Q

How does non - disjunction occur

A

When chromosomes fail to separate in meiosis I and II, gametes end up with more or less chromosome affecting the zygote

30
Q

In 10,000, 800 chromosomally abnormal leads to 750 spontaneous miscarriage

A
31
Q

If more then one chromosome duplicates, it leads to miscarriage

A
32
Q

Down syndrome

A

Usually lethal other then 21 chromosome trisomy

33
Q

Hay flick lucite

A

No. Of times a normal cell divides before cell division stops

34
Q

What is the Chromosome difference btw humans and chimps

A

A fussion of no. 2 chromosomes in chimps

Humans have lot of duplications in non coding regions

35
Q

If X and Y undergo non disjunction

A

Not fatal
3rd in inactive
May be infertile

36
Q

Tellings of karyotypes

A

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
Q

Disorders associated with number mutations

A

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
Q

Function of satellite DNA

A

Highly repetitive short DNA sequence

Ensure stability and protection of centromere region