Fig. 18-19b
Fertilization,
translation
of bicoid
mRNA
Bicoid protein in early
embryo
Anterior end
Bicoid mRNA in mature
unfertilized egg
100 µm
RESULTS
Slide 92
Fig. 18-19c
bicoid mRNA
Nurse cells
Egg
Developing egg
Bicoid mRNA in mature
unfertilized egg
Bicoid protein
in early embryo
CONCLUSION
Slide 93
This phenotype suggests that the product of the mother’s bicoid gene is concentrated at the future anterior end
This hypothesis is an example of the gradient hypothesis, in which gradients of substances called morphogens establish an embryo’s axes and other features
Slide 94
The bicoid research is important for three reasons:
– It identified a specific protein required for some early steps in pattern formation
– It increased understanding of the mother’s role in embryo development
– It demonstrated a key developmental principle that a gradient of molecules can determine polarity and position in the embryo
Slide 95
Concept 18.5: Cancer results from genetic changes that affect cell cycle control
The gene regulation systems that go wrong during cancer are the very same systems involved in embryonic development
Slide 96
Cancer can be caused by mutations to genes that regulate cell growth and division
Tumor viruses can cause cancer in animals including humans
Slide 97
Oncogenes and Proto-Oncogenes
Oncogenes are cancer-causing genes
Proto-oncogenes are the corresponding normal cellular genes that are responsible for normal cell growth and division
Conversion of a proto-oncogene to an oncogene can lead to abnormal stimulation of the cell cycle
Slide 98
Fig. 18-20
Normal growth-
stimulating
protein in excess
New
promoter
DNA
Proto-oncogene
Gene amplification:
Translocation or
transposition:
Normal growth-stimulating
protein in excess
Normal growth-
stimulating
protein in excess
Hyperactive or
degradation-
resistant protein
Point mutation:
Oncogene
Oncogene
within a control element
within the gene
Slide 99
Proto-oncogenes can be converted to oncogenes by