Lecture #15:  Control Systems in Plants

I.  INTRODUCTORY REMARKS

1.  Growth and development in plants are controlled by complex internal responses to environmental conditions.

2.  Plants have the capacity to respond to the direction of light and gravity, and to sense the time of day and time of year.

3.  Most of their internal control systems are regulated by hormones.

4.  A hormone is a chemical messenger that is produced by one part of a multicellular organism and then translocates (usually via fluids) to other parts where it triggers responses in "target" cells and tissues.

5.  A hormone may act on target cells by:

a.  changing the composition of membranes.

b.  causing the depolarization of membranes.

c.  affecting the activity of existing enzymes.

d.  altering the expression of genes.

6.  The responses of plant cells to hormones are elongation, division, and differentiation.

7.  The action of a given hormone is not consistent. The response elicited depends on:

a.  its site of action.

b.  the stage of plant development,

c.  the concentration of the hormone (many hormones have a "biphasic" effect).

 

II.  SIGNAL TRANSDUCTION IN PLANTS

A.  INTRODUCTORY REMARKS

1.  Signal transduction in both plants and animals starts when some energy change in the internal or external environment of the organism affects some type of cellular receptor.

2.  Signal transduction usually involves reception, signal transduction, and cellular response.  (Fig. 39.2)

 

B.  GREENING OF A PLANT AS AN EXAMPLE OF CELL-SIGNAL PROCESSING

1.  Reception:

a.  Receptors undergo conformational changes in response to specific stimuli such as light.

b.  Phytochrome is the cytosolic light receptor for greening.

2.  Transduction:

a.  Transduction is carried out (and amplified) by internally produced chemicals called “second messengers.”

b.  Transduction by way of the cGMP pathway:  (Fig. 39.3)

(i)  transduction begins when phytochrome-activated receptors interact with guanine-binding proteins (G-proteins). 

(ii)  this leads to displacement of guanosine diphosphate with guanosine triphosphate (GTP) on the G-protein.

(iii)  the activated G-protein activates guanyl cyclase.

(iv)  the activated guanyl cyclase converts cyclic guanosine triphosphate (cGTP) to cGMP, a specific second messenger.

(v)  cGMP activates specific protein kinases that activate other proteins by phosphorylation.

c.  Transduction by way of the Ca++ pathway:  (Fig. 39.3)

(i)  activated phytochrome can also react with other G-proteins that can activate calcium ion channels in the plasma membrane.

(ii)  the influx of Ca++ now functions as a “second messenger” that is taken up by a cytoplasmic protein called calmodulin.

(iii)  the Ca++-calmodulin complex activates a calmodulin-dependent kinase.


 

3.  Response:  (Fig. 39.3)

a.  The cellular response is basically a response to kinase activity.

b.  Sometimes, kinases activate cytoplasmic enzymes and cause a cellular response.

c.  Othertimes, the kinase activates transcription factor(s) that promote transcription and translation of specific genes.

     

III. EXPERIMENTS LEADING TO THE DISCOVERY OF PLANT HORMONES

1. Grassy plants have seeds that germinate and give rise to coleoptiles.

2. Microscopic evidence now shows that auxin acts in coleoptiles by causing epidermal cells on shaded side to elongate.  (Fig 39.4)

3. Charles and Francis Darwin (1880) did pioneer work leading to evidence that hormones stimulate plant growth.  (Fig 39.4)

4. Peter Boysen-Jensen (1913) demonstrated the growth substance was mobile.  (Fig 39.4)

5. F.W. Went (1926) extracted the chemical messenger (for growth) onto agar.  (Fig 39.5)

6. Kenneth Thimann (Cal Tech) eventually purified it and determined structure (IAA).

7. Now, there are a number of synthetic compounds that act in the same way.

 

IV.  FUNCTIONS OF THE SIX MAJOR CLASSES OF PLANT HORMONES  (Table 39.1)

A.  AUXIN stimulates cell elongation.

1.  In both roots and stems, it has a biphasic effect, with higher concn inhibiting elongation (due to ethylene formation).

2.  Auxin is actively transported down side of shoot opposite light source. (non-ionized form enters cells)

B.  CYTOKININS stimulate cytokinesis, i.e., cell division (by mitosis), and germination

C.  GIBBERELLINS stimulate growth in seeds and stem buds (promote germination and flowering)

D.  ABSCISSIC ACID slows growth and prepares plants for winter (terminates petiole)

E.  ETHYLENE promotes fruit ripening (as a gas, it spreads to other fruits) (causes aging of plants)

F.  BRASSINOSTEROIDS inhibits root growth, retards abscission, promotes xylem development.

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