AP axis by bicoid and nanos Flashcards
How AP axis genes identified?
Maternal genes responsible for establishment of Drosophila axes were identified using mutants by Nusslein-Volhard and Weishaus. Found anterior, posterior and terminal mutants and hence were able to identify the affected genes.
What were the defects of anterior mutants?
Had tip of the head but not the whole head
What are the anterior genes?
Bicoid, hunchback, exuperantia, swallow, staufen
What were the defects of posterior mutants?
Missing large parts of abdomen
What are the posterior genes?
Nanos, tudor, oskar, vasa, valois, pumilo, caudal
What were the defects of terminal mutants?
Lack most of anterior and posterior structures
What are the terminal genes?
Torso and trunk
Which of these genes are most critical for formation of AP axis?
Bicoid and nanos
Where is bicoid mRNA located? Why?
At the anterior tip of the unfertilised egg due mRNA complex attaching to dynein proteins once in oocyte that are maintained at MTOC at anterior end.
Where is nanos mRNA located? Why?
Trapped at posterior end of oocyte by passive diffusion, binds to cytoskeleton through 3’ UTR.
What happens to bicoid and nanos mRNA?
Bicoid and nanos mRNAs get translated into protein in the egg. The proteins acts as morphogens - diffuse in the syncitial blastoderm forming opposing gradients that are critical for AP patterning.
How do we know Bicoid is related to AP patterning?
- Bicoid gradient is highest at the anterior - suggest anterior development
- Embryos lacking bicoid have no head.
- Embryos injected with bicoid mRNA get ectopic head at site of injection. (Area around injection becomes thorax, supports concentration dependent signal).
How do we know Nanos is related to AP patterning?
- Highest at posterior end
- If no nanos, no abdomen.
Also represses translation of uniformly distributed maternal gene hunchback and so hunchback is anteriorly expressed.
Summarise
Nanos and Bicoid are maternal mRNA distributed at opposite ends of the oocyte, therefore when translated, the proteins produced act as morphogens. They create opposing gradients, the concentrate of which determine AP polarity.
They target zygotic segmentation genes, therefore differing concentrations of the proteins determine expression of different zygotic genes. The zygotic genes are responsible for segmental identity.