The Arabidopsis ADP-ribosylation factor (ARF) and ARF-like (ARL) system and its regulation by BIG2, a large ARF-GEF

Michael Nielsen; Jacob Albrethsen; Flemming Hofmann Larsen; K. Skriver

doi:10.1016/j.plantsci.2006.07.002

The Arabidopsis ADP-ribosylation factor (ARF) and ARF-like (ARL) system and its regulation by BIG2, a large ARF-GEF

Michael Nielsen, Jacob Albrethsen, Flemming Hofmann Larsen, K. Skriver

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

14 Citationer (Scopus)

Abstract

Udgivelsesdato: December 2006

Originalsprog	Engelsk
Tidsskrift	Plant Science
Vol/bind	171
Udgave nummer	6
Sider (fra-til)	707-717
ISSN	0168-9452
DOI	https://doi.org/10.1016/j.plantsci.2006.07.002
Status	Udgivet - 2006

Bibliografisk note

Keywords: Arabidopsis ARF and ARL proteins; Sec7 ARF–GEFs; Catalysis of GDP/GTP exchange

Adgang til dokumentet

10.1016/j.plantsci.2006.07.002

Citationsformater

@article{3cefc5a06c3711dcbee902004c4f4f50,

title = "The Arabidopsis ADP-ribosylation factor (ARF) and ARF-like (ARL) system and its regulation by BIG2, a large ARF-GEF",

abstract = "ADP-ribosylation factor (ARF) and ARF-like (ARL) proteins are small GTPases that undergo a GDP/GTP nucleotide exchange cycle. ARF proteins are important regulators of cellular trafficking. Knowledge of plant ARF proteins and their regulators is emerging from genetic and cellular studies. The Arabidopsis BIG2 ARF-guanine nucleotide exchange factor (GEF) gene is expressed in several tissues and the encoded protein is a typical Arabidopsis ARF-GEF. We address here the specificity of BIG2 for different Arabidopsis ARF proteins. The in vitro effect of the catalytic Sec7 domain of BIG2 on the guanine nucleotide exchange rate of five ARF and ARL proteins was measured using real time fluorescence spectroscopy. The Sec7 domain catalyzed nucleotide exchange on ARF1, but had essentially no effect on the exchange rate of ARF8, ARF9, ARL1, and ARL8a. In Western blots with an anti-BIG2 polyclonal antibody, a BIG2 fraction was detected in membranes, especially those deriving from the Golgi apparatus. The activity of the BIG2 Sec7 domain was unaffected by the Sec7 inhibitor brefeldin A, suggesting that BIG2 is a BFA-insensitive GEF for ARF1 or a close homolog. These studies contribute to our understanding of the biochemical and physiological specificity of ARF and ARF-GEF interactions in plants.",

author = "Michael Nielsen and Jacob Albrethsen and Larsen, {Flemming Hofmann} and K. Skriver",

note = "Keywords: Arabidopsis ARF and ARL proteins; Sec7 ARF–GEFs; Catalysis of GDP/GTP exchange",

year = "2006",

doi = "10.1016/j.plantsci.2006.07.002",

language = "English",

volume = "171",

pages = "707--717",

journal = "Plant Science",

issn = "0168-9452",

publisher = "Elsevier Ireland Ltd",

number = "6",

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TY - JOUR

T1 - The Arabidopsis ADP-ribosylation factor (ARF) and ARF-like (ARL) system and its regulation by BIG2, a large ARF-GEF

AU - Nielsen, Michael

AU - Albrethsen, Jacob

AU - Larsen, Flemming Hofmann

AU - Skriver, K.

N1 - Keywords: Arabidopsis ARF and ARL proteins; Sec7 ARF–GEFs; Catalysis of GDP/GTP exchange

PY - 2006

Y1 - 2006

N2 - ADP-ribosylation factor (ARF) and ARF-like (ARL) proteins are small GTPases that undergo a GDP/GTP nucleotide exchange cycle. ARF proteins are important regulators of cellular trafficking. Knowledge of plant ARF proteins and their regulators is emerging from genetic and cellular studies. The Arabidopsis BIG2 ARF-guanine nucleotide exchange factor (GEF) gene is expressed in several tissues and the encoded protein is a typical Arabidopsis ARF-GEF. We address here the specificity of BIG2 for different Arabidopsis ARF proteins. The in vitro effect of the catalytic Sec7 domain of BIG2 on the guanine nucleotide exchange rate of five ARF and ARL proteins was measured using real time fluorescence spectroscopy. The Sec7 domain catalyzed nucleotide exchange on ARF1, but had essentially no effect on the exchange rate of ARF8, ARF9, ARL1, and ARL8a. In Western blots with an anti-BIG2 polyclonal antibody, a BIG2 fraction was detected in membranes, especially those deriving from the Golgi apparatus. The activity of the BIG2 Sec7 domain was unaffected by the Sec7 inhibitor brefeldin A, suggesting that BIG2 is a BFA-insensitive GEF for ARF1 or a close homolog. These studies contribute to our understanding of the biochemical and physiological specificity of ARF and ARF-GEF interactions in plants.

AB - ADP-ribosylation factor (ARF) and ARF-like (ARL) proteins are small GTPases that undergo a GDP/GTP nucleotide exchange cycle. ARF proteins are important regulators of cellular trafficking. Knowledge of plant ARF proteins and their regulators is emerging from genetic and cellular studies. The Arabidopsis BIG2 ARF-guanine nucleotide exchange factor (GEF) gene is expressed in several tissues and the encoded protein is a typical Arabidopsis ARF-GEF. We address here the specificity of BIG2 for different Arabidopsis ARF proteins. The in vitro effect of the catalytic Sec7 domain of BIG2 on the guanine nucleotide exchange rate of five ARF and ARL proteins was measured using real time fluorescence spectroscopy. The Sec7 domain catalyzed nucleotide exchange on ARF1, but had essentially no effect on the exchange rate of ARF8, ARF9, ARL1, and ARL8a. In Western blots with an anti-BIG2 polyclonal antibody, a BIG2 fraction was detected in membranes, especially those deriving from the Golgi apparatus. The activity of the BIG2 Sec7 domain was unaffected by the Sec7 inhibitor brefeldin A, suggesting that BIG2 is a BFA-insensitive GEF for ARF1 or a close homolog. These studies contribute to our understanding of the biochemical and physiological specificity of ARF and ARF-GEF interactions in plants.

U2 - 10.1016/j.plantsci.2006.07.002

DO - 10.1016/j.plantsci.2006.07.002

M3 - Journal article

VL - 171

SP - 707

EP - 717

JO - Plant Science

JF - Plant Science

SN - 0168-9452

IS - 6

ER -