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双鸟苷酸环化酶在盘基网柄菌体细胞进化过程中的新作用。

Emerging roles for diguanylate cyclase during the evolution of soma in dictyostelia.

作者信息

Kawabe Yoshinori, Du Qingyou, Narita Takaaki B, Bell Craig, Schilde Christina, Kin Koryu, Schaap Pauline

机构信息

Molecular Cell and Developmental Biology, School of Life Sciences, University of Dundee, Dundee, DD15EH, UK.

Department of Life Science, Faculty of Advanced Engineering, Chiba Institute of Technology, Chiba, 275-0016, Japan.

出版信息

BMC Ecol Evol. 2023 Oct 6;23(1):60. doi: 10.1186/s12862-023-02169-z.

Abstract

BACKGROUND

Cyclic di-guanylate (c-di-GMP), synthesized by diguanylate cyclase, is a major second messenger in prokaryotes, where it triggers biofilm formation. The dictyostelid social amoebas acquired diguanylate cyclase (dgcA) by horizontal gene transfer. Dictyostelium discoideum (Ddis) in taxon group 4 uses c-di-GMP as a secreted signal to induce differentiation of stalk cells, the ancestral somatic cell type that supports the propagating spores. We here investigated how this role for c-di-GMP evolved in Dictyostelia by exploring dgcA function in the group 2 species Polysphondylium pallidum (Ppal) and in Polysphondylium violaceum (Pvio), which resides in a small sister clade to group 4.

RESULTS

Similar to Ddis, dgcA is upregulated after aggregation in Ppal and Pvio and predominantly expressed in the anterior region and stalks of emerging fruiting bodies. DgcA null mutants in Ppal and Pvio made fruiting bodies with very long and thin stalks and only few spores and showed delayed aggregation and larger aggregates, respectively. Ddis dgcA- cells cannot form stalks at all, but showed no aggregation defects. The long, thin stalks of Ppal and Pvio dgcA- mutants were also observed in acaA- mutants in these species. AcaA encodes adenylate cyclase A, which mediates the effects of c-di-GMP on stalk induction in Ddis. Other factors that promote stalk formation in Ddis are DIF-1, produced by the polyketide synthase StlB, low ammonia, facilitated by the ammonia transporter AmtC, and high oxygen, detected by the oxygen sensor PhyA (prolyl 4-hydroxylase). We deleted the single stlB, amtC and phyA genes in Pvio wild-type and dgcA- cells. Neither of these interventions affected stalk formation in Pvio wild-type and not or very mildly exacerbated the long thin stalk phenotype of Pvio dgcA- cells.

CONCLUSIONS

The study reveals a novel role for c-di-GMP in aggregation, while the reduced spore number in Pvio and Ppal dgcA- is likely an indirect effect, due to depletion of the cell pool by the extended stalk formation. The results indicate that in addition to c-di-GMP, Dictyostelia ancestrally used an as yet unknown factor for induction of stalk formation. The activation of AcaA by c-di-GMP is likely conserved throughout Dictyostelia.

摘要

背景

环二鸟苷酸(c-di-GMP)由二鸟苷酸环化酶合成,是原核生物中的一种主要第二信使,可触发生物膜形成。盘基网柄菌属的社会性变形虫通过水平基因转移获得了二鸟苷酸环化酶(dgcA)。分类群4中的盘基网柄菌(Ddis)利用c-di-GMP作为分泌信号来诱导柄细胞分化,柄细胞是支持繁殖孢子的原始体细胞类型。我们在此通过探索dgcA在第2类物种苍白聚孢霉(Ppal)和紫聚孢霉(Pvio)中的功能,研究了c-di-GMP的这一作用在盘基网柄菌目中是如何进化的,Pvio位于与分类群4相邻的一个小姐妹进化枝中。

结果

与Ddis相似,dgcA在Ppal和Pvio聚集后上调,主要在新出现的子实体的前部区域和柄中表达。Ppal和Pvio中的dgcA基因敲除突变体形成的子实体具有非常长且细的柄,且孢子很少,分别表现出聚集延迟和聚集体更大的现象。Ddis dgcA-细胞根本无法形成柄,但未表现出聚集缺陷。在这些物种的acaA-突变体中也观察到了Ppal和Pvio dgcA-突变体的长而细的柄。AcaA编码腺苷酸环化酶A,它介导c-di-GMP对Ddis中柄诱导的作用。其他促进Ddis中柄形成的因素包括聚酮合酶StlB产生的DIF-1、氨转运蛋白AmtC促进的低氨以及氧传感器PhyA(脯氨酰4-羟化酶)检测到的高氧。我们在Pvio野生型和dgcA-细胞中删除了单个的stlB、amtC和phyA基因。这些干预措施均未影响Pvio野生型中的柄形成,也未或仅非常轻微地加剧Pvio dgcA-细胞的长细柄表型。

结论

该研究揭示了c-di-GMP在聚集中的新作用,而Pvio和Ppal dgcA-中孢子数量减少可能是间接效应,这是由于延长的柄形成导致细胞池耗尽所致。结果表明,除了c-di-GMP外,盘基网柄菌目在进化过程中还使用了一种未知因子来诱导柄的形成。c-di-GMP对AcaA的激活在整个盘基网柄菌目中可能是保守的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ed6/10559540/10f5ef78ec97/12862_2023_2169_Fig1_HTML.jpg

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