Lin Y., Yang Z.
Department of Plant Biology and Plant Biotechnology Center, Ohio State University, Columbus, Ohio 43210.
Plant Cell. 1997 Sep;9(9):1647-1659. doi: 10.1105/tpc.9.9.1647.
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.
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。