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Department of Ecophysiology

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Elongases involved in suberin bionsynthesis in roots

The role of elongases in the formation of suberin in roots of Arabidopsis

A functional genomics approach is under way in order to identify fatty acid elongase condensing enzymes involved in Arabidopsis root suberin biosynthesis.

 

Principle investigators: Lukas Schreiber and Rochus Franke

 

Summary

Apoplastic depositions of the polyester suberin form physiological important plant-environment interfaces in shoots and roots.  They act as barriers protecting from uncontrolled water loss, nutrient depletion and invasion by pathogens [reviewed in 1].  Furthermore, plants respond to environmental stimuli by modifying the degree of suberization in root cell walls.  Despite the physiological importance of suberin a great gap in our knowledge exists about genes involved in suberin biosynthesis and deposition.  This is primarily due to the lack of appropriate molecular genetic attributes of the investigated species.  As a basis for molecular genetic approaches we established the tissue distribution and chemical composition of root suberin from Arabidopsis [2].  Arabidopsis suberin is characterized by oxygenated and partially unsaturated very long chain fatty acid derivatives.  The chain-length distribution ranging from C16 to C24, indicates that fatty acid elongases (FAE) are essential for suberin biosynthesis.  The FAE1-like gene family of β-KETOACYL-CoA SYNTHASES (KCS) is investigated for their potential involvement in root suberin biosynthesis by determination of the spatial and responsive expression pattern and biochemical suberin phenotyping of insertion mutants.

 

 

Support

This work is supported by the Deutsche Forschungsgemeinschaft (D.F.G.).

 

References

  1. Franke R, Schreiber L. (2007) Suberin – a biopolyester forming apoplastic plant interfaces. Current Opinion in Plant Biology 10: 252-259 (Abstract)
  2. Franke R, Briesen I, Wojciechowski T, Faust A, Yephremov A, Nawrath C, Schreiber L (2005) Apoplastic polyesters in Arabidopsis surface tissues - A typical suberin and a particular cutin. Phytochemistry 66: 2643-2658 (Abstract)

 

The Arabidopsis Gene Family of β-KETOACYL-CoA SYNTHASES (KCS)

AGI code

Name as published

Project Name

Root expression

Assumed function; Ref. /

Products of catalytic function; Ref.

cDNA’s
from Root1

ROOT derived EST / ALL EST

MPSS Signals2
[rel. signature abundance]

Root vs. tissue with highest signature abundance

Microarray3

Σ root expression signals

tissue expression
[% of root expression signal]

 

 

 

 

 

 

At1g01120

KCS1

FAE-KCS1

2/20

 12 : 215 (slique)

2483

coretex & endodermis stage 3 (31%)

Wax biosynthesis

Todd et al. 1999
Suberin biosynthesis

own results /

C20/C20:1, C22, C24, C26;

Todd et al. 1999

At1g04220

FAE-KCS17

1/7

 24 : 295 (slique)

128

endodermis stage 3 (27%)

Suberin biosynthesis

own results /

C22; C24;

Trenkamp et al. 2004

At1g07720

FAE-KCS3

0/17

 3 : 203 (slique)

135

no differential expression

Unknown

At1g19440

FAE-KCS4

4/9

 53 : 42 (slique)

2074

coretex & endodermis stage 3 (12%)

Suberin biosynthesis

Own results

At1g25450

CER60

FAE-KCS5

0/5

 5 : 244 (inflorescence)

688

epidermis stage 2 (21%)

Wax biosynthesis

Hooker et al. 2002 /

C20:1, C26, C28, C30;

Trenkamp et al. 2004

At1g68530

CER6/CUT1

FAE-KCS6

0/62

 3 : 962 (inflorescence)

188

no differential expression

Wax biosynthesis

Millar et al. 1999 /

 

At1g71160

FAE-KCS7

NO EST

 0: 31 (inflorescence)

128

no differential expression

Unknown

At2g15090

FAE-KCS8

1/10

 2 : 53 (inflorescence)

285

no differential expression

Unknown

At2g16280

FAE-KCS9

0/21

 25 : 26 (inflorescence)

2675

no differential expression

Unknown

At2g26250

FDH

FAE-KCS10

0/78

 24 : 868 (inflorescence)

252

epidermis stage 3 (31%)

Cuticle development, trichome formation

Yephremov et al. 1999

At2g26640

FAE-KCS11

1/10

 12 : 10 (inflorescence)

1173

epidermis stage 2 (15%)

Unknown

At2g28630

FAE-KCS12

 

 0 : 292 (inflorescence)

83

no differential expression

Unknown

At2g46720

HIC

FAE-KCS13

One EST that also matches At3g10280

 0 : 18 (inflorescence)

215

endo stage 3 (15%)

Cuticle/stomatal development

Gray et al. 2000

At3g10280

FAE-KCS14

One EST that also matches At2g46720

 0 : 18 (inflorescence)

 Not on affychip

 

Unknown

At3g52160

FAE-KCS15

0/1

 0 : 144 (inflorescence)

233

no differential expression

Unknown

At4g34250

FAE-KCS16

0/8

 0 : 0

105

epidermis stage 1 (26%)

Unknown

At4g34510

KCS2

FAE-KCS2

0/3

 0 : 22 (inflorescence)

55

rootcap (23%)

 

Wax biosynthesis

Clemens&Kunst, 2001 /

C20, C20:1, C24, C26,

Clemens&Kunst, 2001

At4g34520

FAE1

FAE-KCS18

0/22

 0 : 0

209

no differential expression

Seed lipid biosynthesis

James et al. 1995 /

C20, C20:1, C20:2, C22, C22:1

Millar et al. 1997

At5g04530

FAE-KCS21

1/9

 0: 1 (leaf)

105

no differential expression

Unknown

At5g43760

FAE-KCS19

1/16

 195 : 447 (inflorescence)

1442

coretex&endodermis stage 3 (22%)

Unknown

C22, C24

Trenkamp et al. 2004

At5g49070

FAE-KCS20

NO EST

 0 : 11 (inflorescence)

193

no differential expression

Unknown

 

Foot notes:      1 NCBI 2004

                            2 Arabidopsis MPSS

                            3 Birnbaum et al. 2003


 

Letztes Update: 31.08.07 • LS