Department of Biology, Texas A & M University, College Station, Texas 77843.
Genetics. 1986 Jul;113(3):601-19. doi: 10.1093/genetics/113.3.601.
The non-Mendelian erythromycin resistance mutation ery-u1 shows bidirectional uniparental inheritance in crosses between homothallic ery-u1 and ery-u1(+) strains of Chlamydomonas monoica . This inheritance pattern supports a general model for homothallism invoking intrastrain differentiation into opposite compatible mating types and, further, suggests that non-Mendelian inheritance is under mating-type (mt) control in C. monoica as in heterothallic species. However, the identification of genes expressed or required by one gametic cell type, but not the other, is essential to verify the existence of a regulatory mating-type locus in C. monoica and to understand its role in cell differentiation and sexual development. By screening for a shift from bidirectional to unidirectional transmission of the non-Mendelian ery-u1 marker, a mutant with an apparent mating-type-limited sexual cycle defect was obtained. The responsible mutation, mtl-1, causes a 1000-fold reduction in zygospore germination in populations homozygous for the mutant allele and, approximately, a 50% reduction in germination for heterozygous (mtl-1/mtl-1 (+)) zygospores. By next screening for strains unable to yield any viable zygospores in a cross to mtl-1, a second putative mating-type-limited mutant, mtl-2, was obtained. The mtl-2 strain, although self-sterile, mates efficiently with mtl-2(+) strains and shows a unidirectional uniparental pattern of inheritance for the ery-u1 cytoplasmic marker, similar to that observed for crosses involving mtl-1. Genetic analysis indicates that mtl-1 and mtl-2 define unique unlinked Mendelian loci and that the sexual cycle defects of reduced germination (mtl-1) or self-sterility (mtl-2) cosegregate with the effect on ery-u1 cytoplasmic gene transmission. By analogy to C. reinhardtii, the mtl-1 and mtl-2 phenotypes can be explained if the expression of these gene loci is limited to the mt(+) gametic cell type, or if the wild-type alleles at these loci are required for the normal formation and/or functioning of mt( +) gametes only.
非孟德尔红霉素抗性突变体 ery-u1 在同型交配的 ery-u1 和 ery-u1(+) 小单衣藻菌株之间的杂交中表现出双向单向遗传。这种遗传模式支持了一种通用的同型交配模型,即菌株内分化为相反的相容交配型,并且进一步表明非孟德尔遗传受交配型(mt)控制在 C. monoica 中与异配物种相同。然而,鉴定一个配子细胞类型表达或需要的基因,但不是另一个,对于验证 C. monoica 中调节交配型基因座的存在以及理解其在细胞分化和性发育中的作用至关重要。通过筛选非孟德尔 ery-u1 标记物从双向向单向传递的转变,获得了一个具有明显交配型限制的性周期缺陷的突变体。负责的突变 mtl-1 导致突变纯合子群体中合子孢子发芽率降低 1000 倍,并且大约降低了异合子(mtl-1/mtl-1(+))合子孢子的发芽率 50%。通过接下来筛选无法在与 mtl-1 的杂交中产生任何有活力的合子孢子的菌株,获得了第二个假定的交配型限制突变体 mtl-2。mtl-2 菌株虽然自交不育,但与 mtl-2(+) 菌株有效交配,并表现出与涉及 mtl-1 的杂交相似的 ery-u1 细胞质标记物的单向单亲遗传模式。遗传分析表明,mtl-1 和 mtl-2 定义了独特的非连锁孟德尔基因座,并且发芽减少(mtl-1)或自交不育(mtl-2)的性周期缺陷与 ery-u1 细胞质基因传递的影响相分离。与 C. reinhardtii 类似,如果这些基因座的表达仅限于 mt(+)配子细胞类型,或者如果这些基因座的野生型等位基因仅对 mt(+)配子的正常形成和/或功能是必需的,则可以解释 mtl-1 和 mtl-2 表型。