early embryonic development
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Early Embryonic Development. Maternal effect gene products set the stage by controlling the expression of the first embryonic genes. Transcription factors Receptors Regulatory proteins Maternal effect gene products form a gradient of concentration across the embryo. Zygotic Genes. - PowerPoint PPT PresentationTRANSCRIPT
Early Embryonic DevelopmentMaternal effect gene products set the stage by
controlling the expression of the first embryonic genes.
1. Transcription factors2. Receptors3. Regulatory proteinsMaternal effect gene products form a gradient of
concentration across the embryo.
Zygotic GenesZygotic genes are the first genes expressed by the
embryo in response to signals from the maternal effect genes.
The first of these genes are broadly classed into two categories, segmentation genes and selector genes.
Zygotic Genes
Segmentation genesSegmentation genes 1. Divide the embryo into segments 2. Define the number, size and polarity of each
segment.
Zygotic Genes
Selector genesSelector genes specify the identity or fate of each segment.
Segment FormationSegmentation is controlled by three classes of genes:1. Gap proteins2. Pair-rule genes3. Segment polarity genesThese gene products act in a coordinated fashion to
divide the embryo into segments, then create an orientation within the segments.
DevelopmentOnce the segments have been formed, selector genes
are activated and specify the developmental fate of cells within the segment.
Selector genes determine the structures that will ultimately form.
Genetics and CancerNormal cell function and cell lifespan is closely
regulated by careful regulation of the timing of cell division.
Cancer is, at its core, unregulated tissue growth: 1) Uncontrolled cell division2) Metastasis, or spread, of cancer cells away from
their original site to other locations in the body.
Mutations and CancerMutations that influence the development and
progression of cancer can be small or large:1. Small changes, such as a single base mutation or
frameshift mutation that results in an abnormal protein.
2. Large changes such as chromosomal losses, gains or rearrangements, or integration of viral genomes into chromosomes.
Mutations and CancerMutations will always arise at some spontaneous rate
because of inherent imperfections in the DNA replication process.
Carcinogens are environmental substances that impair the replication process at some level such that mutations are introduced at a rate above baseline and promote the formation of cancer.
Known Mutagens and CarcinogensIonizing radiationVirusesEnvironmental chemicals
Typically, more than one mutational event must occur.
Cancer Susceptibility GenesCancer is known to run in families, though usually
there is no clear-cut pattern of inheritance.
Individuals may inherit a mutant alelle that predisposes them to cancer (increases risk of developing cancer) by influencing the age of onset and severity of cancer.
Cell CycleThe phases of the cell cycle are the G1, S, G2
(interphase) and M phases. Some cell types continuously move through the cell
cycle (skin, GI tract lining), dividing at regular intervals.
Other cell types move through the cell cycle only intermittently.
Some cell types withdraw from the cell cycle and enter a permanently non-dividing state called G0.
Cell CycleProgression from one phase to the next is tightly
controlled.Cell-cycle checkpoints are the places in the cell
cycle in which progression are regulated. The major checkpoints are at the transitions from1) G1 to S2) G2 to M3) M (transition into anaphase)
Cell-Cycle RegulationAny mutation that interferes with regulation of the
cell cycle is a candidate carcinogen.De-regulation of the cell-cycle disrupts the ability of
a cell to control its division and increases the probability of unrestricted cell growth.
Control of Cell DivisionControl of cell division is both negative and positive.1. Inhibition of cell division (tumor suppressor
genes)2. Promotion of cell division (protooncogenes)
Tumor Suppressor GenesUnder normal circumstances, tumor suppressor
genes halt progression through the cell cycle. For cell division to occur, these gene products must be absent or inactivated.
If tumor suppressor genes become permanently inactivated or deleted, control of cell division is lost and the cell enters uncontrolled proliferation.
Usually, both alleles must be mutant for tumor suppressor activity to be lost.. (One normal copy is enough to suppress cell division) Recessive
Major Tumor SuppressorsRetinoblastoma gene (Rb): Controls the G1 to S
transition. Although it is always expressed such that the protein is normally present, cells can make the G1/S transition only when Rb is inactivated by phosphorylation.
Wilms tumor gene (WT): Encodes a transcription factor that controls cell division, although the precise function is unknown.
Major Tumor Suppressor Genesp53: A transcription factor involved in cell cycle
arrest, DNA repair and induction of apoptosisapoptosis (programmed cell death). At least 20 genes are known to be regulated by p53, and as much as 50% of all cancers are thought to be associated with malfunctions in p53.
BRCA1/BRCA2: Breast cancer susceptibility genes, thought to be involved in DNA repair mechanisms.
ProtooncogenesWhen these genes are activated, they promote cell
division. For cell division to be “turned off,” these genes must
be absent or inactivated. If protooncogenes are permanently “turned on,” the
cells enter into uncontrolled proliferation.
Major ProtooncogenesProtooncogenes are the normal form of oncogenes.
Oncogenes are the mutant alleles that cause cancer by promoting uncontrolled cell growth.
Typically, only one mutant allele is sufficient to de-regulate cell growth. (Dominant)
Many oncogenes are identified with viruses.
Major OncogenesSrc: A membrane protein originally identified as the
transforming principle of Rous sarcoma virus (RSV)
Ras: A signal transduction protein that transmits signals from the external cell environment and promotes cell division.
MetastasisMetastasis is invasion of cancer cells into other parts
of the body, where they divide and form secondary tumors.
Metastasis is often what ultimately causes death from cancer.
Cancer cells escape the primary tissue by entering the blood or lymphatic system.
MetastasisTumor cells with high metastatic capacity produce
large amounts of enzymes called metalloproteinasesmetalloproteinases, which digest the extracellular framework and allow the tumor cells to penetrate and migrate.
Normal cells inhibit migration by producing TIMPTIMP, or Tissue Inhibitor of Metalloproteinases. Metastasis occurs when there is not enough TIMP to suppress metalloproteinase activity.