BIOL 2402 A&P II
Lecture Notes : Development and Genetics
Dr. Weis
Development and Heredity :: these notes are a guide, refer to your text book for specifics.
I. Development :: Involves mitosis and Meiosis I, II in the process of gametogenesis, gamete formation.
1. Spermatogenesis
2. Oogenesis
A. Gestation :: period of development, in
humans lasting 280 days.
B. Period of the Egg --> Embryo ::
1. Fertilization :
occurs in the ampulla of the uterine tube and forms a zygote
a. Sperm are capacitated to release acrosomal enzymesb. These enzymes help to digest the zona pellucidac. sperm then penetrate the egg and the oocyte membrane then depolarizes to prevent other sperm from fusing by closing Ca++ channels.d. oocyte completes meiosis II to form OVUMe. Chromosomes of the male & female pronucleus combine to form a zygote (2n)
2. Cleavage :: mitotic divisions of the zygote to create blastomeres (daughter cells)
a. when blastomere # = 16 --> MORULA
b. Blastocyst ==> will have a fluid filled hollow space called the Blastocele and the blastomeres will align into two regions :
1) Trophoblasts will form a single layer of cells that create the outer part of the sphere.
FXN: will provide food and eventually form
the fetal portion of the placenta
2) Inner cell mass : cluster of cells that
will form the embryo
3. Implantation ::
Trophoblasts overlying the inner cell mass will adhere to the endometrium.Certain groups of trophoblasts will begin to digest the uterine cellsso that the blastocyst can burrow into the endometrium.
These cells are called syncytial trophoblasts.
A second group of trophoblasts called cellular trophoblasts will secrete
HCG (Human Chorionic Gonadotropin Hormone) that will cause the corpus luteum to continue to produce progesterone, until the chorion of the embryo takes over.
The inner cell mass will separate from the trophoblasts to create the amniotic
cavity
4. Placentation :: formation of the placenta
Chorion formation from trophoblast will develop finger-like chorionic villi and be associated with the endometrium of the uterus to help form the placenta.
Fxn of placenta -> nutrition, respiration, excretion
endocrine ( HCG, progesterone, estrogen, and relaxin)
II. Embryonic Development ::
A. Embryonic Membranes
1. Chorion :: fetal portion of placenta, will have villi formation2. Amnion :: fluid protection and cushion for fetus3. Yolk sac :: 1st to produce RBC, seeds gonads, part of the GI tract, is Energy source for other species4. Allantois :: basis for umbilical cord, will be part of the urinary bladder
B. Germ Layers :: Primitive Tissues -->
Formation by GASTRULATION, into three tissues
1. Ectoderm :: CNS, skin2. Endoderm :: epithelial lining of hallow organs and formation of associated glands3. Mesoderm :: will form all muscle and connective tissues
C. Fetal Circulation ::
1. Umbilical Artery --> blood flow to the placenta return to the mother
2. Umbilical Vein --> blood return from the placenta from the mother to the fetus
3. Vascular Structures that create shunts ::
a. Ductus Venosus.....bypass liverb. Foramen Ovale .....bypass lungsc. Ductus Arteriosus..bypass lungs
III. Gestation :: prenatal development, divided into 3, 3 month sections each called a Trimester
Organogenesis :: organ formation -->
starts in the first trimester, continues development in the second trimester and systems become functional by the third trimester.
Maternal Changes with Pregnancy :
respiratory .... increased tidal volumecirculatory .... increased blood pressuregi.............. increased nutrient requirementsrenal .......... increased filtrationreproductive ... increased uterine size
IV. Labor Stages ::
a. dilation --> from labor onset to fully dilated cervix: 10cm
contractions start weakly, then incr. in force and frequency.
This is the longest of the labor stage
b. Expulsion --> childbirth
from fully dilated cervix to delivery of infant
crowning ... distention of the vulva by
the infants head
c. Placental --> the placenta detaches from the uterine wall
due to contractions of the uterus and the change in
blood supply (constricted) to the placenta.
HEREDITY ::
Genes --> DNA segments, the blueprints for protein synthesis and therefore enzymes
for chemical reactions
23 pairs of Homologous chromosomes :
22 pairs of autosomes1 pair of sex chromosomes
Chromosomes are paired :: two genes, 1 from each parent
these genes are matched on the same locus on the homologous
chromosomes
and are called ALLELES
Alleles are various forms of 1 gene that code for the same or alternate traits
1. If two alleles controlling a trait are alike then called HOMOZYGOUS
2. If two alleles controlling a trait are different, than called HETEROZYGOUS
3. If an allele masks or suppresses the other allele, then it is DOMINANT, and represented by a capital letter
4. The allele that is masked is RECESSIVE, & is represented by a lower case letter
Genotype :: genetic makeup
Phenotype
:: the way the genotype is expressed, visible traits
Inheritance ::
1. Dominant-Recessive --> the interaction between dominant and recessive traits.
Can
be determined by a Punnett Square that is used to figure out the possible
combinations of genes for
a single trait,
and can also be used to predict the probability
of that trait for the offspring.
Examples of dominant/recessive ...
normal mentation is dominantschizophrenia is homozygous recessivenormal vision is homozygous recessive, and problem visions are dominant traits
See
text or lab book for more traits
2. Incomplete Dominance --> the heterozygous genotype has a phenotype between homozygous dominant & homozygous recessive.
Example :: sickle cell anemia
Ss
has normal RBC and sickle RBC
3. Multiple Allele --> CoDominant, both alleles are expressed if present. Example :: ABO blood group -->
Ia
and Ib :: see lab book, or biology lab book
4. Sex-Linked --> inherent traits determined by genes on the sex chromosomes.
Can be X-linked, or Y-linked
Examples
:: hemophilia, colorblindness, baldness
5. Polygene --> phenotype depends on several genes
Examples :: pigmentation of skin and iris
Genetic Screening :: done on newborns to detect anatomical defects and PKU
Fetal Testing :: Routinely done on pregnant women over 35 yrs old and when suspecting a genetic disorder
Cells are checked for chromosome abnormalities
1. Amniocentesis :: amniotic fluid collected2. Chorionic villi sampling : from placenta3. Blood test
Human Genome Project :
mapping of individual chromosomes---> banding patterns
Useful for detecting genetic disorders and cancers