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formation
• The human Haploid gametes (n = 23)
life cycle
Egg cell
Sperm cell
MEIOSIS FERTILIZATION
Diploid
zygote
(2n = 46)
Multicellular
diploid adults
(2n = 46)
Mitosis and
development
Figure 8.13
Sister chromatids
• Chromosomes contain a
very long DNA molecule
with thousands of genes
– Individual chromosomes are
only visible
during cell division
– They are packaged as Centromere
chromatin
• Before a cell starts
dividing, the
chromosomes are
duplicated
separate
Centromere Sister
– Two daughter chromatids
cells are
produced
– Each has a
complete and Chromosome
distribution
to
identical set of daughter
cells
chromosomes
Figure 8.4C
For Mitosis and Meiosis, chromosomes
replicate only once, during interphase
Cell division is a continuum of dynamic
changes
• In mitosis, the duplicated chromosomes are
distributed into two daughter nuclei
• After the chromosomes coil up, a mitotic spindle
moves them to the middle of the cell
• The sister chromatids then separate and move
to opposite poles of the cell
• The process of cytokinesis divides the cell into
two genetically identical cells
INTERPHASE PROPHASE
Centrosomes Early mitotic Centrosome Fragments Kinetochore
(with centriole pairs) spindle of nuclear
Chromatin envelope
Centrosome Spindle
Nucleolus Nuclear Plasma Chromosome,
envelope membrane consisting of two microtubules
sister chromatids
Figure 8.6
METAPHASE ANAPHASE TELOPHASE AND CYTOKINESIS
TELOPHASE I TELOPHASE II
PROPHASE II METAPHASE II ANAPHASE II
AND CYTOKINESIS AND CYTOKINESIS
Cleavage
furrow
Sister Haploid
chromatids daughter cells
separate forming
PROPHASE PROPHASE I
Tetrad formed
Duplicated Chromosome Chromosome by synapsis of
chromosome replication replication homologous
(two sister chromatids) 2n = 4 chromosomes
Chromosomes Tetrads
METAPHASE align at the align at the METAPHASE I
metaphase plate metaphase plate
Figure 8.20A, B
Down syndrome is a genetic disorder. It is also
called Trisomy 21
Figure 8.20C
Table 8.22
A man with
Klinefelter syndrome
has an extra
X chromosome
• Poor beard
growth
• Breast
development
• Underdeveloped
testes
• A woman with Turner syndrome lacks an X
chromosome
Characteristic
facial
features
Web of
skin
Constriction
of aorta
Poor
breast
development
Under-
developed
ovaries
Figure 8.22B
Alterations of chromosome structure can
cause birth defects and cancer
• Chromosome breakage can lead to
rearrangements that can produce genetic
disorders or cancer
– Four types of rearrangement are deletion,
duplication, inversion, and translocation
Deletion
Duplication
Homologous
chromosomes
Inversion
Reciprocal
translocation
Nonhomologous
chromosomes Figure 8.23A, B
• Chromosomal changes in a somatic cell can
cause cancer
– A chromosomal translocation in the bone
marrow is associated with chronic myelogenous
leukemia
Chromosome 9
Reciprocal
Chromosome 22 translocation
“Philadelphia chromosome”
Figure 8.5
Growing out of control, cancer cells
produce malignant tumors
Lymph
vessels
Tumor
Glandular
tissue
Metastasis
Figure 8.10
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