Department of Biological Sciences, Stanford University, Stanford, CA 94305.
Proc Natl Acad Sci U S A. 1987 Nov;84(22):7861-5. doi: 10.1073/pnas.84.22.7861.
The mitochondrial genome of the S-type male-sterile cytoplasm of maize contains two linear episomes, S1 (6397 base pairs) and S2 (5453 base pairs). The S2 episome contains two large unidentified open reading frames, URF1 (3512 base pairs) and URF2 (1017 base pairs). We have demonstrated that a polypeptide with an apparent molecular mass of 130 kDa is the gene product of URF1. This polypeptide was first detected in Coomassie blue-stained protein gels of cms-S (where cms = cytoplasmic male sterile) but not in those of cms-T, cms-C, or normal mitochondrial proteins. The protein product of a translational fusion containing the 5' end of Escherichia coli lacZ and an internal segment from URF1 of S2 was recognized by antisera raised against the 130-kDa variant polypeptide. The mitochondria of fertile F(1) hybrids of cms-S x Ky21 (the male parent carrying nuclear fertility restoration genes) contain as much of the 130-kDa protein as is found in cms-S mitochondria of sterile plants. Spontaneous fertile cytoplasmic revertants from cms-S in a WF9 nuclear background also synthesized the 130-kDa polypeptide. Therefore, the mere presence or absence of the URF1 gene product of S2 does not determine the fertility status of maize plants, because male sterile and male fertile (nuclear restored and revertant) plants can contain equivalent amounts of the 130-kDa polypeptide.
玉米 S 型细胞质雄性不育的线粒体基因组包含两个线性附加体,S1(6397 个碱基对)和 S2(5453 个碱基对)。S2 附加体包含两个未鉴定的大开放阅读框,URF1(3512 个碱基对)和 URF2(1017 个碱基对)。我们已经证明,一个表观分子量为 130kDa 的多肽是 URF1 的基因产物。该多肽最初在 Coomassie 蓝染色的 cms-S(其中 cms = 细胞质雄性不育)蛋白凝胶中检测到,但在 cms-T、cms-C 或正常线粒体蛋白中未检测到。含有大肠杆菌 lacZ 的 5' 端和 S2 的 URF1 内部片段的翻译融合产物的蛋白产物被针对 130kDa 变异多肽的抗血清识别。来自 cms-S x Ky21(携带核育性恢复基因的雄性亲本)的可育 F1 杂种的线粒体与不育植物的 cms-S 线粒体中发现的 130kDa 蛋白一样多。在 WF9 核背景下,来自 cms-S 的自发可育细胞质回复突变体也合成了 130kDa 多肽。因此,S2 的 URF1 基因产物的存在与否并不决定玉米植株的育性状态,因为雄性不育和可育(核恢复和回复突变体)植物可以含有等量的 130kDa 多肽。