Koonjul P K, Minhas J S, Nunes C, Sheoran I S, Saini H S
Institut de Recherche en Biologie Végétale, Université de Montréal, 4101, rue Sherbrooke est, Montreal H1X 2B2, Canada.
J Exp Bot. 2005 Jan;56(409):179-90. doi: 10.1093/jxb/eri018. Epub 2004 Nov 8.
Water deficit during male meiosis in wheat (Triticum aestivum L.) causes pollen sterility. With a view to identifying the internal trigger for this failure, it was found that water stress specifically impairs the activities of vacuolar and cell-wall invertases in anthers prior to the arrest of pollen development. The enzymes are affected only when water deficit occurs around meiosis. Three invertase cDNAs, two encoding the cell-wall (Ivr1, Ivr3) and one the vacuolar (Ivr5) isoform, were isolated from an anther cDNA library. RNA gel-blot analysis using floral organs of well-watered plants revealed that these genes were expressed preferentially, though not exclusively, in anthers. Semi-quantitative RT-PCR demonstrated that transitory water deficit during meiosis selectively down-regulated the transcription of two of the three genes, one encoding the vacuolar (Ivr5) and the other a cell-wall (Ivr1) isoform, without affecting the Ivr3 message. Their expression did not recover upon resumption of watering. Another homologue of Ivr1 was also down-regulated, but only during the post-stress period. The stress effects on invertase transcripts were consistent with those on the developmental profiles of the corresponding enzyme activities. In situ hybridization revealed that the stress-sensitive invertase genes, unlike an insensitive one, were expressed within the microspores. No evidence for an invertase inhibitor under stress was found. Together the results show that the decline in invertase activity is probably regulated primarily at the transcriptional level in a gene- and cell-specific manner.
小麦(Triticum aestivum L.)雄性减数分裂期间的水分亏缺会导致花粉不育。为了确定这种失败的内在触发因素,研究发现水分胁迫在花粉发育停滞之前会特异性损害花药中液泡和细胞壁转化酶的活性。这些酶仅在减数分裂前后出现水分亏缺时受到影响。从花药cDNA文库中分离出三个转化酶cDNA,其中两个编码细胞壁(Ivr1、Ivr3)同工型,一个编码液泡(Ivr5)同工型。对水分充足的植物花器官进行RNA凝胶印迹分析表明,这些基因优先(但并非唯一)在花药中表达。半定量RT-PCR表明,减数分裂期间的短暂水分亏缺选择性地下调了三个基因中的两个基因的转录,一个编码液泡(Ivr5)同工型,另一个编码细胞壁(Ivr1)同工型,而不影响Ivr3的转录本。恢复浇水后,它们的表达并未恢复。Ivr1的另一个同源物也被下调,但仅在胁迫后阶段。胁迫对转化酶转录本的影响与对相应酶活性发育谱的影响一致。原位杂交显示,与不敏感的转化酶基因不同,对胁迫敏感的转化酶基因在小孢子内表达。未发现胁迫下存在转化酶抑制剂的证据。这些结果共同表明转化酶活性的下降可能主要在转录水平上以基因和细胞特异性方式受到调控。