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控制酵母孢子形成过程中20S RNA合成的新型细胞质遗传元件。

New cytoplasmic genetic element that controls 20S RNA synthesis during sporulation in yeast.

作者信息

Garvik B, Haber J E

出版信息

J Bacteriol. 1978 Apr;134(1):261-9. doi: 10.1128/jb.134.1.261-269.1978.

Abstract

Under conditions that induce meiosis and sporulation in Saccharomyces cerevisiae, most strains accumulate a 20S RNA, amounting to as much as 15% of the newly synthesized RNA. The ability of cells to accumulate this new RNA species depends on a dominant genetic element that is cytoplasmically inherited, but is distinct from the other cytoplasmic elements that have been previously identified. The ability to synthesize 20S RNA does not depend on mitochondrial DNA, 2-micron DNA, the translational suppressor psi, the genetic element carrying URE3, or double-stranded killer RNA. However, all 20S- strains examined were also nonkillers, although many nonkiller strains were 20S+. This work also shows that 20S RNA accumulating is not essential for sporulation even though it is induced only by conditions that initiate sporulation. Furthermore, strains that are unable to complete meiosis are still capable of producing 20S RNA when placed under the nitrogen starvation conditions that promote sporulation.

摘要

在诱导酿酒酵母减数分裂和孢子形成的条件下,大多数菌株会积累一种20S RNA,其含量高达新合成RNA的15%。细胞积累这种新RNA种类的能力取决于一种显性遗传元件,该元件是细胞质遗传的,但与先前鉴定的其他细胞质元件不同。合成20S RNA的能力不依赖于线粒体DNA、2微米DNA、翻译抑制因子psi、携带URE3的遗传元件或双链杀伤RNA。然而,所有检测的20S-菌株也都是非杀伤菌株,尽管许多非杀伤菌株是20S+。这项研究还表明,即使20S RNA仅由引发孢子形成的条件诱导产生,其积累对于孢子形成也不是必需的。此外,无法完成减数分裂的菌株在置于促进孢子形成的氮饥饿条件下时,仍然能够产生20S RNA。

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