Growth factors are made in growing regions, then they move to other tissues to regulate growth in response to stimuli (for example; auxin promotes cell elongation in shoots but inhibits growth in roots)
Indoleacetic acid (IAA) is a type of auxin which brings about plant responses by altering the transcription of genes inside plant cells
Auxins are a group of plant growth factors that influence many aspects of plant growth
IAA is produced in growing regions and is transported via diffusion, active transport, and through the phloem. Its redistribution is influenced by environmental stimuli such as light and gravity, causing uneven growth.
IAA in shoots:
Light causes IAA to move to the shaded side of the shoot (a phototropism response). When light is even, the IAA molecules are evenly distributed.
When light is uneven, the IAA moves towards the shaded side which increases the rate of cell elongation, causing the shaded side to grow at a faster rate, pushing the tip towards the light.
IAA in roots (geotropism):
in roots, high IAA concentration result in a lower rate of cell elongation (opposite of shoot cells). IAA is transported towards the lower side of plant roots, resulting in the lower side growing at a slower rate than the upper side of the root - causing the root to bend downwards (towards centreofgravity)
Auxin stimulates cell signalling cascade:
Auxin binds to receptor in the cell surface membrane of target cell
second inactivemessenger is activated by binding of auxin to receptor
transcriptionfactors are activated by second messenger
mRNA for relevant gene is transcribed - leading to synthesis of relevant protein
genes produce proteins for cell division, expansion and differentiation
Flowering in plants is controlled by the stimulus of night length (some flower when nights are short and some when nights are long)
A phytochrome molecule consists of a protein bonded to a non-protein light-absorbing pigment molecule. The pigment molecule exists in two different isomers (Pr and Pfr)
The Pr inactive form of phytochrome absorbs red light
The Pfr active form of phytochrome absorbs far-red light
Absorption of red light converts Pr into Pfr
Absorption of far-red light converts Pfr into Pr
Pfr accumulates in the light as more red light is absorbed.
In the dark, any Pfr present is slowly converted to Pr
During the day time:
unfiltered sunlight is rich in red light but deficient in far-red light
this means rapid conversion of Pr to Pfr but little conversion of Pfr back to Pr
so Pfr accumulates in the daytime
During the night time:
Pfr slowly decays back into Pr
The ratio of Pfr to Pr allows the plant to determine the length of the night
Phytochromes regulate responses such as:
seed germination
stem elongation
chlorophyll formation
flowering
length of day = photoperiod
Pfr promotes flowering in long day plants
Pfr inhibits flowering in short day plants
short day plants flower in the winter as nights are longer, which means that there is time for more Pfr to be converted back into Pr so little Pfr remains - inhibiting flowering
long day plants flower in the summer as the nights are shorter, which means that there is little time for all Pfr to be converted back to Pr, so Pfr remains to promote flowering
High levels of Pfr activates flowering; it binds to receptors and activates expression of genes that stimulate flowering, so the active gene is transcribed and translated into a protein that causes flowers to be produced.