Department of Biology, Box 355325, University of Washington, Seattle, Washington 98195-5325, USA.
J Exp Bot. 2011 May;62(8):2715-30. doi: 10.1093/jxb/erq441. Epub 2011 Jan 25.
In maize (Zea mays L.), chloroplast development progresses from the basal meristem to the mature leaf tip, and light is required for maturation to photosynthetic competence. During chloroplast greening, it was found that chloroplast DNA (cpDNA) is extensively degraded, falling to undetectable levels in many individual chloroplasts for three maize cultivars, as well as Zea mexicana (the ancestor of cultivated maize) and the perennial species Zea diploperennis. In dark-grown maize seedlings, the proplastid-to-etioplast transition is characterized by plastid enlargement, cpDNA replication, and the retention of high levels of cpDNA. When dark-grown seedlings are transferred to white light, the DNA content per plastid increases slightly during the first 4 h of illumination and then declines rapidly to a minimum at 24 h during the etioplast-to-chloroplast transition. Plastid autofluorescence (from chlorophyll) continues to increase as cpDNA declines, whereas plastid size remains constant. It is concluded that the increase in cpDNA that accompanies plastid enlargement is a consequence of cell and leaf growth, rather than illumination, whereas light stimulates photosynthetic capacity and cpDNA instability. When cpDNA from total tissue was monitored by blot hybridization and real-time quantitative PCR, no decline following transfer from dark to light was observed. The lack of agreement between DNA per plastid and cpDNA per cell may be attributed to nupts (nuclear sequences of plastid origin).
在玉米(Zea mays L.)中,叶绿体的发育从基生分生组织向成熟叶片尖端进行,光对于成熟到具有光合作用能力是必需的。在叶绿体的绿色化过程中,人们发现叶绿体 DNA(cpDNA)被广泛降解,在三个玉米品种、玉米的祖先 Zea mexicana 和多年生物种 Zea diploperennis 中,许多单个叶绿体中的 cpDNA 水平降至无法检测的水平。在黑暗中生长的玉米幼苗中,前质体向叶绿体的转变以质体增大、cpDNA 复制和高 cpDNA 水平的保留为特征。当黑暗中生长的幼苗被转移到白光下时,在最初的 4 小时的光照期间,每个质体的 DNA 含量略有增加,然后在质体向叶绿体转变的 24 小时内迅速下降到最小值。质体自发荧光(来自叶绿素)随着 cpDNA 的下降而继续增加,而质体大小保持不变。可以得出结论,伴随着质体增大的 cpDNA 的增加是细胞和叶片生长的结果,而不是光照,而光照刺激了光合作用能力和 cpDNA 的不稳定性。当通过印迹杂交和实时定量 PCR 监测总组织中的 cpDNA 时,在从黑暗转移到光照后没有观察到下降。每个质体的 DNA 与每个细胞的 cpDNA 之间缺乏一致性可能归因于 nupts(质体起源的核序列)。