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

A

Lignin

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
Q

Sperm + Egg = Zygote

A

Axial division (Meristem + root)

26
Q

Axial division

A

Apical ——
Central
Hypophysis
suspensor

27
Q

Apical ——>
Central ——>
Hypophysis ——>
suspensor ——>

A

Apical ——> cotyledons
Central ——> hypocotyl
Hypophysis ——> root cap
suspensor ——>

28
Q

Gus gene

A

code for Beta-glucuronidases

29
Q

Beta-glucuronidases

A

catalyze breakdown of complex carbohydrates. leads plant embryonic cell formation and differentiation

30
Q

Position-dependence of GUS expression –

A

cells do not have a ‘fixed’ fate during embryogenesis

31
Q

PIN
• Protein that forms part of the complex that
transports auxin

A

• 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
Q

Gene essential for embryogenesis

A

Gnom gene
Gurke gene
Fackel gene
monopteros

33
Q

Gnom gene [GT]

A

GT. Controls apical/basal polarity [Terminal - on both ends]

34
Q

Gurke gene

A

Ga. Controls norman apical region organization (apical)

35
Q

Fackel gene

A

FC. controls body organization [central]

36
Q

monopteros

A

MB. controls primary formation of roots/vascular tissue [basal]

37
Q

SAM

A

Shoot apical meristem.

The tiny leaves that surround the meristem are called leaf primordia

38
Q

IAA

A

An accumulation of the hormone auxin promotes leaf initiation

39
Q

Genetic control of leaf identity.

How does a leafprimordiumbecome a leaf,rather than part of the meristem?

A

Cells in the meristem are indeterminate

KNOX-1 genes maintain the meristem in an indeterminate state

40
Q

KNOX-1

A

accumulates in the meristem but not the leaf primordia

41
Q

KNOX genes act in part by stimulating cytokinin synthesis

A

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
Q

Overexpression of KNOX-1 genes

A

increases leaf complexity and indeterminacy

43
Q

Primordium-specific genes promote differentiation

A

•“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
Q

The activities of ARP and KNOX-1 genes are mutually antagonistic

A

The two classes of transcription factors are mutually repressive, and help establish a separate identity for the emerging leaf primordium

45
Q

Expression of KNOX1 transcription factors correlates with leaf complexity

A

In plants with simple leaves, KNOX1 expression remains off in leaf primordia