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Cell Differentiation:
cells are genetically programmed to be specialized and will assume unique structural & functional attributes Fertilized Egg = totipotential stem cells vs. pleuripotential stem cells
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Oocyte with sperm = fertilization
Zygote=fertilized egg
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Series of mitotic divisions = cleavage
2-cell stage (30 hours post fertilization)
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Zygote 2-Cell Morula Cells
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8-Cell Stage…
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Morula= solid ball of cells (32 cells +)
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Blastocyst=hollow ball of cells, implants in
uterus 6-7 days after fertilization ( cells) Trophoblast= Chorion placenta Inner cell mass= embryo + amniotic sac
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Embryonic disk develops from inner cell mass
gastrulation= endoderm Somites mesoderm ectoderm (2nd week) = embryonic stage
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Endoderm (inner layer)=
-respiratory system -Pharnyx (throat) -Pancreas -Liver -GI tract Mesoderm (middle)= -gonads -kidneys -circulatory system -Somites = muscles, skeleton
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Ectoderm (outer layer)=
-skin -hair -inner ear -lens of eye -nervous system -connective tissues
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Neurulation= nervous system forms
(3rd week) (2mm long)
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Spina Bifida
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Anencephaly
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Extraembryonic Membranes
Trophoblast= placenta + chorion Inner cell mass= embryo + amniotic sac + allantois (bladder & umbilicus) + yolk sac (nutrients & germ cells)
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4th week= Organogenesis
-heart begins to beat (70 bpm) [2.5 billion beats per 70 years] -5 mm long -susceptible to teratogens [thalidomide]
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2nd Month = Morphogenesis
-arms, legs, tail bone form -25 mm long -major organs continue to form 6 week embryo
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7th week= sexual differentiation occurs
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8th week embryo becomes a “fetus”
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-most major organs are formed -placenta takes over pregnancy
End of 1st trimester -most major organs are formed -placenta takes over pregnancy 2nd trimester (175 mm; 225 gm) -organs grow -nervous system continues development 3rd trimester -baby grows rapidly! -6th month=1.3 lbs; 1 ft long
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What controls growth & development? GENES!
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Hutchinson-Gilford Syndrome (Progeria)
8 year old child with Hutchinson-Gilford Syndrome (Progeria)
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Homeotic Genes (Hox)= act as switches and control pattern formation
during development Dermatomes
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Mutations: changes made in normal genetic sequence of DNA
A. Cells have DNA repair mechanisms but… ~ 1 out of 1 billion mutations aren’t repaired B. If change affects last nucleotide of codon = okay if 1st codon affected = bad Why? [Overhead] C. Mutagens: agents which cause mutations (e.g., radiation… UV-B, X-rays, sodium nitrite, cigarettes
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Mutations Point mutations: one nitrogen base gets substituted for another. Ex. DNA normally read as…. …GGTCTTCTC… UV radiation zaps and changes message to…. …GGTCATCTC The result is Valine gets substituted for Glutamine… causing the disease….
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Sickle Cell Anemia
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Sickle Cell Anemia:
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e.g. Sickle Cell Anemia HbA HbS HbA/HbA HbA/HbS HbS/HbS
¼ normal; ½ sickle cell trait; ¼ sickle cell anemia
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Sickle Cell Anemia and Malaria
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Malaria & Sickle Cell Allele Distribution
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Mutations b. Frame-shift: an extra nucleotide gets slipped into message… THE CAT RAN FAR….. THE QCA TRA NFA R c. Insertions: extra messages added THE FAT CAT RAN FAR d. Deletions: messages removed THE RAN FAR
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A Deletion Mutation…
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Mutations: e. Trisomy: extra chromosomes are added to our “Karyotype” = usually lethal
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Trisomy 21 and Down’s Syndrome
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