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显微注射抗Rop1Ps抗体抑制花粉管伸长表明Rho型GTP酶在顶端生长控制中起关键作用。

Inhibition of Pollen Tube Elongation by Microinjected Anti-Rop1Ps Antibodies Suggests a Crucial Role for Rho-Type GTPases in the Control of Tip Growth.

作者信息

Lin Y., Yang Z.

机构信息

Department of Plant Biology and Plant Biotechnology Center, Ohio State University, Columbus, Ohio 43210.

出版信息

Plant Cell. 1997 Sep;9(9):1647-1659. doi: 10.1105/tpc.9.9.1647.

Abstract

Microinjection of anti-Rop1Ps antibodies was used to assess the function of a tip-localized Rho-type GTPase, Rop, in controlling pollen tube growth. Injected antibodies induced sustained growth arrest within 1 to 2 min after injection but did not affect cytoplasmic streaming. Coinjection with Rop rescued antibody-induced growth inhibition, indicating that injected antibodies specifically block the activity of Rop GTPases. Antibody-induced inhibition was significantly enhanced in the presence of a lower threshold of extracellular [Ca2+] or a subinhibitory dosage of caffeine. In contrast, injection of the C3 toxin, which inactivates a different Rho-type GTPase, arrested tube elongation 10 to 20 min after injection. C3-induced growth arrest was accompanied by the cessation of cytoplasmic streaming. These data suggest that Rho-type GTPases play a pivotal role in the control of pollen tube elongation. We propose that Rop may regulate a Ca2+-dependent pathway involved in vesicle docking/fusion, whereas a C3-sensitive Rho GTPase may mediate cytoplasmic streaming.

摘要

通过显微注射抗Rop1Ps抗体来评估一种位于花粉管顶端的Rho型小GTP酶Rop在控制花粉管生长中的功能。注射的抗体在注射后1至2分钟内诱导花粉管持续生长停滞,但不影响胞质环流。与Rop共同注射可挽救抗体诱导的生长抑制,这表明注射的抗体特异性地阻断了Rop小GTP酶的活性。在细胞外[Ca2+]阈值较低或咖啡因亚抑制剂量存在的情况下,抗体诱导的抑制作用显著增强。相反,注射使另一种Rho型小GTP酶失活的C3毒素后,花粉管在注射后10至20分钟停止伸长。C3诱导的生长停滞伴随着胞质环流的停止。这些数据表明,Rho型小GTP酶在控制花粉管伸长中起关键作用。我们推测,Rop可能调节参与囊泡对接/融合的Ca2+依赖途径,而C3敏感的Rho小GTP酶可能介导胞质环流。

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