Asexual Reproduction in Hydra. Hydra “budding” a form of asexual reproduction.
Fig. 13-2a (a) Hydra 0.5 mm Bud Parent. DNA – lots of it in a small space chromatin Chromosome...
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Transcript of Fig. 13-2a (a) Hydra 0.5 mm Bud Parent. DNA – lots of it in a small space chromatin Chromosome...
![Page 1: Fig. 13-2a (a) Hydra 0.5 mm Bud Parent. DNA – lots of it in a small space chromatin Chromosome Know how to label.](https://reader034.fdocuments.us/reader034/viewer/2022051621/56649e9f5503460f94ba0f7c/html5/thumbnails/1.jpg)
Fig. 13-2a
(a) Hydra
0.5 mm
Bud
Parent
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DNA – lots of it in a small space
chromatin
ChromosomeKnow how to
label
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Fig. 12-UN3
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Fig. 12-14
SG1
M checkpoint
G2M
Controlsystem
G1 checkpoint
G2 checkpoint
Cyclins are proteins that control the cell cycle.They create chemical“checkpoints”through-out the process.
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Fig. 12-UN1
Telophase andCytokinesis
Anaphase
Metaphase
Prometaphase
Prophase
MITOTIC (M) PHASE
Cytokinesis
Mitosis
SG1
G2
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Fig. 12-9
Cleavage furrow100 µm
Contractile ring ofmicrofilaments
Daughter cells
(a) Cleavage of an animal cell (SEM) (b) Cell plate formation in a plant cell (TEM)
Vesiclesformingcell plate
Wall ofparent cell
Cell plate
Daughter cells
New cell wall
1 µm
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What is the haploid number for each? Symbol for haploid? What kindof cells are haploid?
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Fig. 13-3APPLICATION
TECHNIQUE
Pair of homologousreplicated chromosomes
5 µm
Centromere
Sisterchromatids
Metaphasechromosome
The processof creating a graphicdisplay of chromosomesfrom a cell to determineabnormal chromosomenumber. Homologuesare paired up andarranged in descendingorder according to length.
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Fig. 13-4
KeyMaternal set ofchromosomes (n = 3) hapolid #Paternal set ofchromosomes (n = 3)
2n = 6Diploid number
Centromere
Two sister chromatidsof one replicatedchromosome
Two nonsisterchromatids ina homologous pair
Pair of homologouschromosomes(one from each set)
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Fig. 13-5Key
Haploid (n)Diploid (2n)
Haploid gametes (n = 23)
Egg (n)
Sperm (n)
MEIOSIS FERTILIZATION
Ovary Testis
Diploidzygote(2n = 46)
Mitosis anddevelopment
Multicellular diploidadults (2n = 46)
The relationshipbetween mitosisand meiosis
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Fig. 13-12-5Prophase Iof meiosis
Homologouspair
NonsisterChromatids
Centromere
Anaphase I
Anaphase II
Daughtercells
Recombinant chromosomes
TEM
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Fig. 13-9a
MITOSIS MEIOSIS
MEIOSIS I
Prophase IChromosome
replication
Homologouschromosomepair
Chromosomereplication
2n = 6
Parent cell
Prophase
Replicated chromosome
Metaphase Metaphase I
Anaphase ITelophase I
Haploid n = 3
Daughter cells ofmeiosis I
MEIOSIS II
Daughter cells of meiosis IInnnn
2n2n
Daughter cellsof mitosis
AnaphaseTelophase
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Fig. 13-9b
SUMMARY
MeiosisMitosisProperty
DNAreplication
Number ofdivisions
Occurs during interphase beforemitosis begins
One, including prophase, metaphase,anaphase, and telophase
Synapsis ofhomologouschromosomes
Does not occur
Number ofdaughter cellsand geneticcomposition
Two, each diploid (2n) and geneticallyidentical to the parent cell
Role in theanimal body
Enables multicellular adult to arise fromzygote; produces cells for growth, repair,and, in some species, asexual reproduction
Occurs during interphase before meiosis I begins
Two, each including prophase, metaphase, anaphase, andtelophase
Occurs during prophase I along with crossing overbetween nonsister chromatids; resulting chiasmatahold pairs together due to sister chromatid cohesion
Four, each haploid (n), containing half as many chromosomesas the parent cell; genetically different from the parentcell and from each other
Produces gametes; reduces number of chromosomes by halfand introduces genetic variability among the gametes
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Fig. 13-UN3
DNA replication
Meiosis I –PMAT to separate homologouspairs. Have2 cells.
Meiosis II – before itstarts, NO DNA replication.PMAT separates sister chromatids. Four haploid cells produced. No pairsof chromosomes.
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Fig. 13-UN4
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NONDISJUCTION
• Failure of a particular chromosome to separate properly during meiosis.
• Can happen in meiosis I if a particular homologous pair fails to separate.
• Can happen in meiosis if sister chromatids of a particular chromosome fail to separate
• Remember the term nondisjunction applies to abnormal gametes. In humans, abnormal egg or sperm would be 24 or 22 chromosomes.
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Fig. 15-13-3
Meiosis I
Nondisjunction
(a) Nondisjunction of homologous chromosomes in meiosis I
(b) Nondisjunction of sister chromatids in meiosis II
Meiosis II
Nondisjunction
Gametes
Number of chromosomes
n + 1 n + 1 n + 1n – 1 n – 1 n – 1 n n
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• Aneuploidy results from the fertilization of a gamete in which nondisjunction occurred• Offspring with this condition have an abnormal number of a particular chromosome
• REMEMBER – aneuploidy means abnormal numberof a particular chromosome in a ZYGOTE (FERTILIZATION HAS HAPPENED). We are not discussing
the gamete any more.
Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Two types of aneuploidy:•Monosomy: A monosomic zygote has only one copy of a particular chromosome. In humans an example would be Turner’s syndrome: Female child only has only 1 sex chromosome (X) in each diploid cell instead of XX, she has a total of 45 chromosomes in diploid cells instead of 46.
•Trisomy: A trisomic zygote has three copies of a particular chromosome. In humans an example would be Down’s Syndrome: Child has 3 copies of chromosome 21 in all diploid cells for a total of 47.
Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Another Trisomic disorder Patau Syndrome (Trisomy 13)
• cleft palate• fetuses with this condition rarely to go to term• so it occurs in only 1 in 6000 live births • It is rare for babies to survive for very long if liveborn because of
the multitude of anomalies • atrial septal defect • inguinal hernia• polydactyly of hands and feet• Sometimes cyclopia or absence of eyes
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Patau Syndrome (Trisomy 13)
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Edward Syndrome (Trisomy 18)• Sometimes due to translocation• Survival rate of Edwards Syndrome is very low • Approximately 95% die in utero. • Of liveborn infants, only 50% live to 2 months, and only 5–10% will survive
their first year of life. • The median life span is five to fifteen days• One percent of children born with this syndrome live to age ten, typically in
cases of the less severe Edwards syndrome.• heart defects at birth • intestines protruding outside the body• Feeding and breathing difficulties• Microcephaly• Clenched fists
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• Polyploidy is a condition in which an organism has more than two complete sets of chromosomes– Triploidy (3n) is three sets of chromosomes– Tetraploidy (4n) is four sets of chromosomes
• Polyploidy is common in plants, but not animals• Polyploids are more normal in appearance than
aneuploids
Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Down Syndrome (Trisomy 21)
• Down syndrome is an aneuploid condition that results from three copies of chromosome 21
• It affects about one out of every 700 children born in the United States
• The frequency of Down syndrome increases with the age of the mother, a correlation that has not been explained
Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Fig. 15-16a
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Fig. 15-16b
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2 processes for collecting fetalcells for karyotyping.
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Aneuploidy of Sex Chromosomes
• Nondisjunction of sex chromosomes produces a variety of aneuploid conditions
• Klinefelter syndrome is the result of an extra chromosome in a male, producing XXY individuals
• Monosomy X, called Turner syndrome, produces X0 females, who are sterile; it is the only known viable monosomy in humans
• Poly X – 3 copies of XXX• Jacob Syndrome - XYY
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•Almost all (95%) have •Short stature •Loss of ovarian function
•Caused by the absence of a set of genes from the short arm of one X chromosome •1 out of every 2,000-2,500 female live births •Single X chromosome
•75-80% single X is contributed by mother •X-O = Female (Turner Syndrome) •X-X-Y=Male (Klinefelter Syndrome)
•Appearance •Short stature
•Absent adolescent growth spurt •Average adult height is 4 feet 8 inches •Loss of SHOX gene necessary for growth of long bones
•Short fingers (4th metacarpal) •Newborns – puffy, bulbous hands and feet
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Alterations of Chromosome Structure
• Breakage of a chromosome can lead to four types of changes in chromosome structure:– Deletion removes a chromosomal segment– Duplication repeats a segment– Inversion reverses a segment within a chromosome– Translocation moves a segment from one
chromosome to another
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Fig. 15-15
DeletionA B C D E F G H A B C E F G H(a)
(b)
(c)
(d)
Duplication
Inversion
Reciprocaltranslocation
A B C D E F G H
A B C D E F G H
A B C D E F G H
A B C B C D E F G H
A D C B E F G H
M N O C D E F G H
M N O P Q R A B P Q R
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Disorders Caused by Structurally Altered Chromosomes
• The syndrome cri du chat (“cry of the cat”), results from a specific deletion in chromosome 5
• A child born with this syndrome is mentally retarded and has a catlike cry; individuals usually die in infancy or early childhood
• Certain cancers, including chronic myelogenous leukemia (CML), are caused by translocations of chromosomes
Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings