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β-glucanase Eng2 is required for ascus wall endolysis after sporulation in the fission yeast Schizosaccharomyces pombe

机译:β-葡聚糖酶Eng2在裂殖酵母裂殖酵母中形成孢子壁后需要内吞

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摘要

Meiosis is the developmental program by which sexually reproducing diploid organisms generate haploid gametes. In yeast, meiosis is followed by spore morphogenesis. WhenSchizosaccharomyces pombe diploid cells undergo meiosis, they differentiate into asci containing four haploid ascospores that are highly resistant to environmental stress. The formation of the ascospore wall requires the activity of several enzymes involved in the biosynthesis and modification of its components, such as α-and β-glucan synthases. Once the spores are completely mature, the wall of the ascus undergoes an endolytic process that results in the release of ascospores from the ascus, allowing their dispersal into the environment. This process requires the activity of the endo-α;-1,3-glucanase Agn2. Here, we focus on the characterization of the endo-β-1,3-glucanase Eng2, which is also required for ascospore release from the ascus. Although Eng2 is present during the mitotic cycle, the protein accumulates after meiosis II. The expression ofeng2+ is required for the efficient release of ascospores, as shown by placingeng2+ under the control of a repressible promoter. Furthermore, a point mutation that destroys the catalytic activity of the protein results in a phenotype similar to that of the mutant strain. Finally, we demonstrate that exogenous addition of purified Eng2 releases the ascospores from asci generated by aneng2δ mutant. We propose that Eng2 would act together with Agn2 to completely hydrolyze the ascus wall, thereby assisting in the release of ascospores in S. pombe. Copyright © 2009, American Society for Microbiology. All Rights Reserved.
机译:减数分裂是有性繁殖二倍体生物体产生单倍体配子的发育程序。在酵母中,减数分裂后是孢子形态发生。当粟酒裂殖酵母二倍体细胞进行减数分裂时,它们分化为包含四个对环境胁迫具有高度抵抗力的单倍体子囊孢子的asci。子囊壁的形成需要参与生物合成和修饰其组分的几种酶的活性,例如α-和β-葡聚糖合酶。孢子完全成熟后,果皮壁会经历内溶过程,从而导致子皮从果皮中释放出来,从而使其散布到环境中。该过程需要内切α; -1,3-葡聚糖酶Agn2的活性。在这里,我们着重于β-内源性β-1,3-葡聚糖酶Eng2的表征,这也是从子囊中释放子囊孢子所必需的。尽管在有丝分裂周期中存在Eng2,但该蛋白在减数分裂II后积聚。 eng2 +的表达是高效释放子囊孢子所必需的,如将eng2 +置于可抑制启动子的控制下所示。此外,破坏蛋白质催化活性的点突变产生与突变菌株相似的表型。最后,我们证明纯化的Eng2的外源添加从aneng2δ突变体产生的asci中释放了子囊孢子。我们建议Eng2将与Agn2共同作用,以完全水解Ascus壁,从而帮助在Pombe中释放子囊孢子。版权所有©2009,美国微生物学会。版权所有。

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