Tata Institute of Fundamental Research, Department of Biological Sciences, Mumbai, India.
Int J Dev Biol. 2020;64(1-2-3):21-28. doi: 10.1387/ijdb.190290mj.
The strategies and experimental approaches that led the author to demonstrate the role of auxin in caulonema differentiation in the protonema of the moss Funaria hygrometrica are discussed. In stationary suspension cultures, the status of cell differentiation is regulated by inoculum cell density and auxin level. At low inoculum cell densities, 2-5 µM indole acetic acid (IAA) led to the differentiation of 65-70% caulonema filaments in 5-6 days. Caulonema can also differentiate in auxin-free medium if buffered at pH 5.0 after a lag of 6±1 days. The duration of lag can be manipulated and the cells are capable of responding to auxin at a higher level (3-10 µM) and produce about 20% caulonema after 3 days. This responsiveness or sensitivity to auxin can be enhanced further by growing cells in a nutrient-limited medium buffered at pH 5.0. In this medium, addition of 3 µM IAA led to the differentiation of 75-80% caulonema and rhizoids within 3 to 4 days. Work done in other laboratories has shown that auxin promotes caulonema differentiation in the moss Physcomitrella patens by positively regulating two basic helix-loop-helix type of transcription factor genes namely root hair defective six-like1 (PpRSL1) and PpRSL2 (Jang and Dolan 2011, New Phytologist 192: 319-327).
讨论了作者证明生长素在藓类植物水灰藓原丝体中的 caulonema 分化中的作用的策略和实验方法。在静止悬浮培养中,细胞分化状态受接种细胞密度和生长素水平的调节。在低接种细胞密度下,2-5 μM 吲哚乙酸(IAA)导致 65-70%的 caulonema 丝在 5-6 天内分化。如果在 pH5.0 下缓冲, caulonema 也可以在无生长素的培养基中分化,滞后 6±1 天。滞后时间可以被操纵,细胞能够在更高的生长素水平(3-10 μM)下做出反应,并在 3 天后产生约 20%的 caulonema。通过在 pH5.0 下缓冲的营养受限培养基中培养细胞,可以进一步增强对生长素的这种响应性或敏感性。在这种培养基中,添加 3 μM IAA 可在 3 至 4 天内将 75-80%的 caulonema 和根状茎分化出来。其他实验室的工作表明,生长素通过正向调节两种基本螺旋-环-螺旋类型的转录因子基因,即根毛缺陷六型 1(PpRSL1)和 PpRSL2,促进藓类植物 Physcomitrella patens 中的 caulonema 分化(Jang 和 Dolan,2011,新植物学家 192:319-327)。