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ORGANOGENESIS
VULVA FORMATION IN CAENORHABDITIS ELEGANS
PRESENTED BY
MD KADER MULLAH
ORGANOGENESIS
INTRODUCTION: The production and
development of organs after the formation of
three germ layers in embryo is know as
ogranogenesis.
VULVA FORMATION IN CAENORHABDITIS ELEGANS
a. Mostly caenorhabditis elegans individuals are
hermaphrodites.
b. In early development-they are male and gonad
produces sperm.
c. When they grow old- they develop ovaries.
• Formation of vulva in caenorhabditis elegans
is simply a case in which one inductive signal
generates a variety of cell types.
• This organ forms during the larval stage from
six cells called vulva precursor cells.
• The cell connecting the overlying gonad to the
vulval precursor cells is called anchor cell.
• The anchor cell secretes the LIN-3 protein, a
paracrine factor(similar to mammalian
epidermal growth factor , or EGF) that
activates the RTK (receptor tyrosine kinase
pathway).
• If the anchor cell is destroyed the PVCs will
not form a vulva but instead become part of
the hypodermis(skin).
• The six VPCs influenced by the anchor cell
form an equivalenve group.
• Each member of this group is competent to
become induced by the anchor cell and can
assume any of the three fates,depending on
its proximity of the anchor cell.
• The cell directly beneath the anchor cell
divides to form the central vulval cells.
• The two cells flanking that central cell divide
to become the lateral vulval cells , while the
three cells farther away from the anchor cell
generate hypodermal cells.
• If the anchor cell is destroyed , all six cells of
the equivalence group divide once and
contribute to the hypodermal tissue.
• If the three central VPCs are destroyed , the
three outer cells , which normally form
hypodermis , generate vulval cells instead.
• The LIN-3 protein is received by the LET-23
receptor tyrosine kinase on the VPCs , and
the signal is transferred to the nucleus
through the RTK pathway. The target of the
kinase cascade is the LIN-31 protein.
• When this protein is phosphorylated in the nucleus , it loses
its inhibitory protein partner and is able to function as a
transcription factor , promoting vulval cell fates.
MECHANISM
• The LIN-3 protein forms a concentration gradient.
here , the VPC closest to the anchor cell, receives
the highest concentration of LIN-3 protein and
generates the central vulval cells.The two VPCs
adjacent to it (P5.p and P7.p) receive a lower amount
ofb LIN-3 and become the lateral vulval cells. The
VPCs farther away from the anchor cell do not
receive enough LIN-3 to have an effect, so they
become hypodermis.
THANK YOU EVERYBODY
ORGANOGENESIS

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ORGANOGENESIS

  • 1. ORGANOGENESIS VULVA FORMATION IN CAENORHABDITIS ELEGANS PRESENTED BY MD KADER MULLAH
  • 2. ORGANOGENESIS INTRODUCTION: The production and development of organs after the formation of three germ layers in embryo is know as ogranogenesis.
  • 3. VULVA FORMATION IN CAENORHABDITIS ELEGANS a. Mostly caenorhabditis elegans individuals are hermaphrodites. b. In early development-they are male and gonad produces sperm. c. When they grow old- they develop ovaries.
  • 4. • Formation of vulva in caenorhabditis elegans is simply a case in which one inductive signal generates a variety of cell types. • This organ forms during the larval stage from six cells called vulva precursor cells. • The cell connecting the overlying gonad to the vulval precursor cells is called anchor cell.
  • 5. • The anchor cell secretes the LIN-3 protein, a paracrine factor(similar to mammalian epidermal growth factor , or EGF) that activates the RTK (receptor tyrosine kinase pathway). • If the anchor cell is destroyed the PVCs will not form a vulva but instead become part of the hypodermis(skin).
  • 6. • The six VPCs influenced by the anchor cell form an equivalenve group. • Each member of this group is competent to become induced by the anchor cell and can assume any of the three fates,depending on its proximity of the anchor cell. • The cell directly beneath the anchor cell divides to form the central vulval cells.
  • 7. • The two cells flanking that central cell divide to become the lateral vulval cells , while the three cells farther away from the anchor cell generate hypodermal cells. • If the anchor cell is destroyed , all six cells of the equivalence group divide once and contribute to the hypodermal tissue.
  • 8. • If the three central VPCs are destroyed , the three outer cells , which normally form hypodermis , generate vulval cells instead. • The LIN-3 protein is received by the LET-23 receptor tyrosine kinase on the VPCs , and the signal is transferred to the nucleus through the RTK pathway. The target of the kinase cascade is the LIN-31 protein.
  • 9.
  • 10. • When this protein is phosphorylated in the nucleus , it loses its inhibitory protein partner and is able to function as a transcription factor , promoting vulval cell fates.
  • 11. MECHANISM • The LIN-3 protein forms a concentration gradient. here , the VPC closest to the anchor cell, receives the highest concentration of LIN-3 protein and generates the central vulval cells.The two VPCs adjacent to it (P5.p and P7.p) receive a lower amount ofb LIN-3 and become the lateral vulval cells. The VPCs farther away from the anchor cell do not receive enough LIN-3 to have an effect, so they become hypodermis.