Chapter 19: Auxin: The Growth Hormone Flashcards

1
Q

phototropism

A

The bending of plants toward light. This phenomenon is caused by differential growth

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2
Q

The youngest leaves are sheathed in a protective

organ called the coleoptile.

A

Coleoptiles are very sensitive to light, especially to blue light

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3
Q

The Principal Auxin in Higher Plants Is

Indole-3-Acetic Acid

A

IAA biosynthesis is associated with rapidly dividing and rapidly growing tissues, especially in shoots. Although virtually all plant tissues appear to be capable of producing low levels of IAA, shoot apical meristems, young leaves, and developing fruits and seeds are the primary sites of IAA synthesis

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4
Q

IAA moves mainly from the apical to the basal end (basipetally) in excised oat coleoptile sections.

A

This type of unidirectional transport is termed polar transport. Auxin is the only plant growth hormone known to be transported polarly

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5
Q

The standard method for measuring polar auxin transport. The polarity of transport is independent of orientation with respect to gravity.

A

The longitudinal gradient of auxin from the shoot to the root affects various developmental processes, including stem elongation, apical dominance, wound healing, and leaf senescence

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6
Q

Polar Transport Requires Energy and Is Gravity

Independent

A

Roots grow from the basal ends of these bamboo
sections, even when they are inverted. The roots form at the basal end because polar auxin transport in the shoot is independent of gravity

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7
Q

Polar transport proceeds in a cell-to-cell fashion, rather than via the symplast.

A

That is, auxin exits the cell through the plasma membrane, diffuses across the compound middle lamella, and enters the cell below through its plasma membrane

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8
Q

The loss of auxin from cells is termed auxin

efflux; the entry of auxin into cells is called auxin uptake or influx.

A

The overall process requires metabolic energy, as evidenced by the sensitivity of polar transport to O2 deprivation and metabolic inhibitors.

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9
Q

Auxin influx. The first step in polar transport is auxin

influx. According to the model, auxin can enter plant cells from any direction by either of two mechanisms:

A
  1. Passive diffusion of the protonated (IAAH) form
    across the phospholipid bilayer
  2. Secondary active transport of the dissociated (IAA–) form via a 2H+–IAA– symporter
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10
Q

The dual pathway of auxin uptake arises because the passive permeability of the membrane to auxin depends strongly on the apoplastic pH.

A

The undissociated form of indole-3-acetic acid, in which the carboxyl group is protonated, is lipophilic and readily diffuses across lipid bilayer membranes

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11
Q

Plant Cell Wall

A

Determine plant structure
Cell Wall glues cells together
Exoskeleton
Bulk flow requires cell walls

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12
Q

Beta-D-glucan chain

A

generates Cellulose microfibril

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13
Q

CesA —–> Rosette subunit ——> Rosette

A

Cellulose (makes up cell wall)

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14
Q

UDP-G

A

Donates glucose to the growing glucan chain in cellulose synthesis

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15
Q

Tip growth

A

confined to apical domain

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16
Q

Diffused growth

A

spread growth across

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17
Q

turgor pressure

A

extends cell wall

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18
Q

Galactomannan

A

From Guar gum —- Thickening agent

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19
Q

Secondary cell wall

20
Q

Randomly oriented cellulose microfibrils

A

Randomly equal in all direction = sphere shape

21
Q

Transverse oriented cellulose microfibrils

A

same direction = square

22
Q

Fertilization =

A

Endosperm —-> seed —–> fruit developement

Sperm + Egg = Zygote

23
Q

double fertilization

A

Flowering plants

Sperm + Egg = Zygote (+) 2nd fertilization = Triploid endosperm nucleus

24
Q

angiosperm embryogenesis forms

A

Embryonic axis + 2 cotyledons

25
Sperm + Egg = Zygote
Axial division (Meristem + root)
26
Axial division
Apical ------ Central Hypophysis suspensor
27
Apical ------> Central ------> Hypophysis ------> suspensor ------>
Apical ------> cotyledons Central ------> hypocotyl Hypophysis ------> root cap suspensor ------>
28
Gus gene
code for Beta-glucuronidases
29
Beta-glucuronidases
catalyze breakdown of complex carbohydrates. leads plant embryonic cell formation and differentiation
30
Position-dependence of GUS expression –
cells do not have a ‘fixed’ fate during embryogenesis
31
PIN • Protein that forms part of the complex that transports auxin
• PIN family of proteins are an ancestral family of proteins that regulate the transport of auxin in and out of the ER • Another family of PINs are involved in the membrane transport of auxin out of the basal ends of conducting cells.
32
Gene essential for embryogenesis
Gnom gene Gurke gene Fackel gene monopteros
33
Gnom gene [GT]
GT. Controls apical/basal polarity [Terminal - on both ends]
34
Gurke gene
Ga. Controls norman apical region organization (apical)
35
Fackel gene
FC. controls body organization [central]
36
monopteros
MB. controls primary formation of roots/vascular tissue [basal]
37
SAM
Shoot apical meristem. | The tiny leaves that surround the meristem are called leaf primordia
38
IAA
An accumulation of the hormone auxin promotes leaf initiation
39
Genetic control of leaf identity. How does a leafprimordiumbecome a leaf,rather than part of the meristem?
Cells in the meristem are indeterminate KNOX-1 genes maintain the meristem in an indeterminate state
40
KNOX-1
accumulates in the meristem but not the leaf primordia
41
KNOX genes act in part by stimulating cytokinin synthesis
STM1--->IPT--->CK mutant (stm1) fails to initiate a shoot apical meristem. This mutant can be rescued by CK application or by expression of the cytokininbiosynthesis IPT gene at the SAM. STM is a transcription factor that induces expression of an IPT gene.
42
Overexpression of KNOX-1 genes
increases leaf complexity and indeterminacy
43
Primordium-specific genes promote differentiation
•“ARP” is derived from three genes, ASYMMETRIC LEAF1, ROUGH SHEATH2, and PHANTASTICA * ARP genes encode MYB transcription factors * Expressed in cells of leaf primordia * Promote determinate growth and differentiation
44
The activities of ARP and KNOX-1 genes are mutually antagonistic
The two classes of transcription factors are mutually repressive, and help establish a separate identity for the emerging leaf primordium
45
Expression of KNOX1 transcription factors correlates with leaf complexity
In plants with simple leaves, KNOX1 expression remains off in leaf primordia