Barnes S A, Nishizawa N K, Quaggio R B, Whitelam G C, Chua N H
Laboratory of Plant Molecular Biology, Rockefeller University, New York, New York 10021-6399,USA.
Plant Cell. 1996 Apr;8(4):601-15. doi: 10.1105/tpc.8.4.601.
We have characterized a far-red-light response that induces a novel pathway for plastid development in Arabidopsis seedlings. This response results in the inability of cotyledons to green upon subsequent white light illumination, and the response is suppressed by exogenous sucrose. Studies with mutants showed that this far-red block of greening is phytochrome A dependent and requires an intact downstream signaling pathway in which FHY1 and FHY3 may be components but in which HY5 is not. This highlights a previously undefined branchpoint in the phytochrome signaling pathway. Ultrastructural analysis showed that the far-red block correlates with both the failure of plastids to accumulate prolamellar bodies and the formation of vesicles in the stroma. We present evidence that the far-red block of greening is the result of severe repression of protochlorophyllide reductase (POR) genes by far-red light coupled with irreversible plastid damage. This results in the temporal separation of phytochrome-mediated POR; repression from light-dependent protochlorophyllide reduction, two processes that normally occur in coordination in white light.
我们已经鉴定出一种远红光反应,该反应在拟南芥幼苗中诱导了一条质体发育的新途径。这种反应导致子叶在随后的白光照射下无法变绿,并且该反应受到外源蔗糖的抑制。对突变体的研究表明,这种远红光对变绿的阻断依赖于光敏色素A,并且需要完整的下游信号通路,其中FHY1和FHY3可能是其组成部分,但HY5不是。这突出了光敏色素信号通路中一个以前未定义的分支点。超微结构分析表明,远红光阻断与质体积累原片层体的失败以及基质中囊泡的形成有关。我们提供的证据表明,远红光对变绿的阻断是远红光对原叶绿素酸酯还原酶(POR)基因的严重抑制以及质体不可逆损伤的结果。这导致了光敏色素介导的POR抑制与光依赖性原叶绿素酸酯还原在时间上的分离,这两个过程通常在白光下协同发生。