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CELS191 lecture 14, 15 and 16 - includes description of all stages of the cycle, terminology around chromosomes/genes, differences between mitosis and meiosis, and errors that can occur
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Karyotype
An ordered, visual representation of the chromosomes in a cell stopped at metaphase.
Cell cycle
interphase & mitotic phase
Interphase
G1 (growth), S (DNA duplication), G2 (preparation for cell divison)
Mitotic (M) phase
telophase and cytokinesis
G2 phase
two centrosomes form
nuclear envelope intact
nucleolus visible
DNA not yet condensed
Mitosis phases
prophase, prometaphase, metaphase, anaphase, telophase & cytokinesis
Prophase
nucleoli disappear
duplicated DNA condenses
mitotic spindle forms
microtubules lengthen
centrosomes move to opposite poles
Kinetochore microtubules
microtubules that attach to kinetochores
Nonkinetochore microtubules
lengthen the cell by interacting with those from the opposite pole of the spindle
Prometaphase
nuclear envelope breaks down
kinetochores form
Mitotic spindle
structure composed microtubules that separates duplicated chromosomes
Kinetochore
a protein structure that forms on the centromere of a chromosome. Point of attachment for microtubules.
Metaphase
centrosomes at opposite poles
kinetochore microtubules attach
chromosomes line up at metaphase plate (homologous pairs do not interact)
Anaphase
ends when two poles of cell contain identical and complete collections of chromosomes
sister chromatids disjoin:
kinetochore microtubules shorten, moving daughter chromosomes to opposite poles
nonkinetochore microtubules lengthen, elongating cell
Telophase
chromosomes become less condensed
mitotic spindle breaks down
two daughter nuclei form
nucleoli reappear
mitosis (the division of one nucleus into two genetically identical nuclei) is complete
cytokinesis
cytoplasm divides
animals = formation of cleavage furrow which pinches off to give two daughter cells
plants = formation of a cell plate
each daugher cell has…
one copy of each duplicated chromosome
(sister chromatids separate during anaphase and each chromatid becomes a daughter chromosome)
where do homologous pairs disjoin?
chiasmus
where do sister chromatids disjoin?
centromere
Meiosis
production of 4 genetically distinct haploid daughter gametes used for reproduction from diploid parent cell.
Mitosis
cell division that produces two daughter cells identical to each other and to parent cell.
Mitosis function
to produce somatic cells used for growth and repair
Prophase I
homolgous chromosomes undergo synapsis and crossing over
Metaphase I
homologous pairs/chiasmata align at metaphase plate
Anaphase I
homologous pairs are separated
Telophase I
duplicated chromsomes (pairs of sister chromatids) reach the poles at opposite ends of the cell
Cytokinesis I
two genetically distinct haploid cells (only one of each pair of the homologous chromosomes)
Prophase II
spindles form, kinetochore microtubules attach
Metaphase II
duplicated chromosomes/pairs of sister chromatids align at metaphase plate
Anaphase II
sister chromatids disjoin
Telophase II & Cytokinesis II
four genetically distinct haploid cells, each with a single set of of unreplicated chromosomes
chiasmata present in…
meiosis I
disjunction occurs between…
chromatids in mitosis and meiosis II, homologous chismata in meiosis I
chromosomal number of resultant cells and genetic make up of resultant cells in mitosis, meiosis I and meiosis II
mitosis (2n → 2n), genetically identical
meiosis I (2n → n), genetically distinct
meiosis II (n→n), genetically distinct
genetic diversity occurs through
independent assortment (meiosis II), crossing over (meiosis I), random fertilization
alignment in mitosis, meiosis I and meiosis II
chromosomes align independently in mitosis and meiosis II), homologous chromosomes synapse (meiosis I)
genetic diversity allows
variable environments, changing environments, reduced sibling competition
number of possible gametes (with different chromosomal combinations)
2^n
Meiotic nondisjunction
failure of chromosomes to separate properly during meiosis
effect of nondisjunction during meiosis I
all 4 gametes affected (n+1, n+1, n-1, n-1), sister chromatids not identical at centromeres.
effect of nondisjunction during meiosis II
only 2 gametes affected (n+1, n-1, n, n)
sister chromatids identical at centromeres
Aneuploidy
zygote has a missing or extra copy of a chromosome
how does aneuploidy arise
gamete with abnormal number of chromosomes fuses with a normal gamete.
monosomy
n-1 gamete fuses with n gamete. zygote is 2n-1, missing one chromosome
trisomy
n+1 gamete fuses with n gamete. zygote is 2n +1, one chromosome is present in triplicate (3 copies)
down syndrome
trisomy 21 - 3 copies of chromosome 21
Klinefelter syndrome
XXY - two copies of X chromosome
Turner syndrome
XO — only one sex chromosome (X)
Polyploidy
possession of two or more complete chromosome sets
polyploidy caused by…
nondisjunction of all chromosomes in one gamete, or the failure of a diploid zygote to divide after replicating its chromosome in the G2 phase.
autopolyploid
self fertilization of a zygote with two incorrect gametes
Deletion
chromosome breaks in one or more places and a segment (deletion) is lost — sister chromatid forms deletion loop as nothing to pair with.
Duplication
when a segment (duplication) is present more than once — can arise when a broken fragment of one chromosome reattaches as an extra segment to a sister or non-sister chromatid
Inversion
segment turned 180 degrees — requires breaks at two points and joining of segments to opposite breakage points — ABCDEF → AEDCBF
Translocations
segment of a chromosome attaches to a non-homologous chromosome — e.g. translocation 14/21