Departments of Agronomy and Vegetable Crops, University of Florida, 32611, Gainesville, FL, USA.
Theor Appl Genet. 1991 Jun;81(6):793-9. doi: 10.1007/BF00224992.
Cloned pearl millet [Pennisetum glaucum (L.) R. Br.] mitochondrial (mt) DNA fragments rearranged by spontaneous reversion from cytoplasmic male sterility (cms) to fertility were characterized by restriction mapping, hybridization with maize mt genes, and transcription analyses. The clones characterized were a 4.7-kb fragment found only in the male-sterile cytoplasm and lost upon reversion to fertility, a 10.9-kb fragment found in all cytoplasms and not changed by reversion, a 13.6-kb fragment found in the male-sterile and -fertile normal cytoplasms and lost in seven of the eight revertants studied, and a 9.7-kb fragment not found in the male-sterile cytoplasm but produced by reversion from male sterility to fertility. The restriction maps verified that the four cloned pearl millet fragments contained two sets of repeated sequences, one on the 4.7-, 10.9-, and 13.6-kb fragments, the other on the 13.6- and 9.7-kb fragments. The rrn18, rrn5, and coxI genes were located in the repeated regions of the 4.7-, 10.9-, and 13.6-kb cloned fragments. The correlation of reversion (eight independent events) with the loss of fragments containing the rrn18, rrn5, and coxI genes suggests that those lost fragments and their gene content could be responsible for the expression of cms. Transcriptional analyses using both Northern blots and end-labeled mtRNA probes verified that transcripts homologous to the rrn18 and coxI genes were present in pearl millet total mtRNA. However, no transcript differences were detected among cms, revertant, and fertile normal cytoplasms, suggesting that the reversion process involves mutational changes that may not affect transcript size. Transcript analyses indicated that the 10.9-kb clone contained an unidentified gene on the end opposite the rrn18 gene; however, since it was present in all cytoplasms, it is not believed to be involved in cms.
克隆的珍珠粟[黍属(Pennisetum glaucum(L.)R. Br.]线粒体(mt)DNA 片段通过细胞质雄性不育(cms)自发回复为可育的重排,通过限制图谱、与玉米 mt 基因杂交和转录分析进行了特征描述。所描述的克隆是一个仅在雄性不育细胞质中发现的 4.7kb 片段,在回复为可育时丢失,一个在所有细胞质中发现的 10.9kb 片段,在回复过程中没有改变,一个在雄性不育和正常细胞质中发现的 13.6kb 片段,在研究的八个回复体中有七个丢失,以及一个在雄性不育细胞质中未发现但通过从雄性不育回复为可育产生的 9.7kb 片段。限制图谱证实,四个克隆的珍珠粟片段包含两组重复序列,一组位于 4.7、10.9 和 13.6kb 片段上,另一组位于 13.6 和 9.7kb 片段上。rrn18、rrn5 和 coxI 基因位于 4.7、10.9 和 13.6kb 克隆片段的重复区域。rrn18、rrn5 和 coxI 基因的回复(八个独立事件)与包含 rrn18、rrn5 和 coxI 基因的片段丢失相关,这表明那些丢失的片段及其基因含量可能负责 cms 的表达。使用 Northern 印迹和末端标记 mtRNA 探针的转录分析证实,rrn18 和 coxI 基因的同源物存在于珍珠粟总 mtRNA 中。然而,在 cms、回复和可育正常细胞质之间没有检测到转录差异,这表明回复过程涉及可能不影响转录大小的突变变化。转录分析表明,10.9kb 克隆在 rrn18 基因相反末端包含一个未知基因;然而,由于它存在于所有细胞质中,因此不认为它与 cms 有关。