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United States Department of Agriculture

Agricultural Research Service

Title: Fragile Fiber3, An Arabidopis Gene Encoding a Type II Inositol Polyphosphate, Is Required for Secondary Wall Synthesis and Actin Organization in Fiber Cells

Authors
item Zheng-Hua, Ye - UNIVERSITY OF GEORGIA
item Morrison Iii, Wiley
item Burk, David - UNIVERSITY OF GEORGIA
item Ruiqin, Zong - UNIVERSITY OF GEORGIA

Submitted to: The Plant Cell
Publication Type: Peer Reviewed Journal
Publication Acceptance Date: September 21, 2004
Publication Date: December 1, 2004
Citation: Zheng-Hua, Y., Morrison III W.H., Burk, D., Ruiqin, Z. 2004. Fragile fiber3, an arabidopis gene encoding a type II inositol polyphosphate, is required for secondary wall synthesis and actin organization in fiber cells. The Plant Cell. 16:3242-3259.

Interpretive Summary: This study demonstrates that a specific gene required for cell wall formation and mechanical strength of fiber cells regulates an enzyme which influences cell wall strength. A mutation of this gene seriously affects the ability of this enzyme to function causing a reduction of cell wall strength and development. Mutations of this enzyme in humans have been shown to cause dramatic effects in development or stress response and a rare X-linked developmental disorder. Understanding the role of genes and their mutations that affect these enzymes provided basic information on cell wall structure and development.

Technical Abstract: Type II inositol polyphosphate 5-phosphatases (5PTases) in yeast and animals have been known to regulate the level of phosphoinositides and thereby influence various cellular activities such as vesicle trafficking and actin organization. In plants, little is known about the phosphatases involved in hydrolysis of phosphoinositides and roles of type II 5PTases in plant cellular functions have not yet been characterized. In this study, we demonstrate that the FRAGILE FIBER3 (FRA3) gene of Arabidopsis thaliana, which encodes a type II 5PTase, plays an essential role in the secondary wall synthesis in fiber cells and xylem vessels. The fra3 mutations caused a dramatic reduction in secondary wall thickness and a concomitant decrease in stem strength. These phenotypes were associated with an alteration in actin organization in fiber cells. Consistent with the defective fiber and vessel phenotypes, the FRA3 gene was found to be highly expressed in fiber cells and vascular tissues in stems. The FRA3 protein is composed of two domains, an N-terminal localized WD-repeat domain and a C-terminal localized 5PTase catalytic domain. In vitro activity assay deomonstrated that recombinant FRA3 exhibited phosphatase activity toward PtdIns(4,5)P2, PtdIns(3,4,5)P3 and Ins(1,4,5)P3 with the highest substrate affinity toward PtdIns(4,5)P2. The fra3 missense mutation, which caused an amino acid substitution in the conserved motif II of the 5PTase catalytic domain, completely abolished the FRA3 phosphatase activity. Moreover, the endogenous levels of PtdIns(4,5)P2 and Ins(1,4,5)P3 were found to be elevated in fra3 stems. Together, our findings suggest that the FRA3 type II 5PTase is involved in the phosphoinositide metabolism and influences secondary wall synthesis and actin organization.

Last Modified: 12/21/2014
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