Tang H V, Chang R, Pring D R
Crop Genetics and Environment Research Unit, U.S. Department of Agriculture-Agricultural Research Service, and Department of Plant Pathology and Plant Molecular and Cellular Biology Program, University of Florida, Gainesville, 32611, USA.
Genetics. 1998 Sep;150(1):383-91. doi: 10.1093/genetics/150.1.383.
Defective nuclear-cytoplasmic interactions leading to aberrant microgametogenesis in sorghum carrying the IS1112C male-sterile cytoplasm occur very late in pollen maturation. Amelioration of this condition, the restoration of pollen viability, involves a novel two-gene gametophytic system, wherein genes designated Rf3 and Rf4 are required for viability of individual gametes. Rf3 is tightly linked to, or represents, a single gene that regulates a transcript processing activity that cleaves transcripts of orf107, a chimeric mitochondrial open reading frame specific to IS1112C. The mitochondrial gene urf209 is also subject to nucleus-specific enhanced transcript processing, 5' to the gene, conferred by a single dominant gene designated Mmt1. Examinations of transcript patterns in F2 and two backcross populations indicated cosegregation of the augmented orf107 and urf209 processing activities in IS1112C. Several sorghum lines that do not restore fertility or confer orf107 transcript processing do exhibit urf209 transcript processing, indicating that the activities are distinguishable. We conclude that the nuclear gene(s) conferring enhanced orf107 and urf209 processing activities are tightly linked in IS1112C. Alternatively, the similarity in apparent regulatory action of the genes may indicate allelic differences wherein the IS1112C Rf3 allele may differ from alleles of maintainer lines by the capability to regulate both orf107 and urf209 processing activities.
携带IS1112C雄性不育细胞质的高粱中,导致异常小孢子发生的核质相互作用缺陷发生在花粉成熟的晚期。改善这种情况,即恢复花粉活力,涉及一种新型的双基因配子体系统,其中名为Rf3和Rf4的基因是单个配子活力所必需的。Rf3与一个调节转录本加工活性的单基因紧密连锁或代表该单基因,该转录本加工活性可切割orf107的转录本,orf107是IS1112C特有的嵌合线粒体开放阅读框。线粒体基因urf209也受到由单个显性基因Mmt1赋予的细胞核特异性增强转录本加工的影响,该加工发生在基因的5'端。对F2和两个回交群体中转录本模式的检测表明,IS1112C中增强的orf107和urf209加工活性共分离。一些不能恢复育性或赋予orf107转录本加工的高粱品系确实表现出urf209转录本加工,这表明这些活性是可区分的。我们得出结论,在IS1112C中,赋予增强的orf107和urf209加工活性的核基因紧密连锁。或者,这些基因在明显调控作用上的相似性可能表明等位基因差异,其中IS1112C的Rf3等位基因可能与保持系的等位基因不同,因为它有能力调节orf107和urf209的加工活性。