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在莱茵衣藻的铵趋化作用中,细胞集体迁移。

Cells collectively migrate during ammonium chemotaxis in Chlamydomonas reinhardtii.

机构信息

Department of Biological Sciences, Louisiana State University, Baton Rouge, LA, 70803, USA.

Laboratory for Chemistry and Life Science, Institute of Innovative Research, Tokyo Institute of Technology, Yokohama, Japan.

出版信息

Sci Rep. 2023 Jul 4;13(1):10781. doi: 10.1038/s41598-023-36818-6.

Abstract

The mechanisms governing chemotaxis in Chlamydomonas reinhardtii are largely unknown compared to those regulating phototaxis despite equal importance on the migratory response in the ciliated microalga. To study chemotaxis, we made a simple modification to a conventional Petri dish assay. Using the assay, a novel mechanism governing Chlamydomonas ammonium chemotaxis was revealed. First, we found that light exposure enhances the chemotactic response of wild-type Chlamydomonas strains, yet phototaxis-incompetent mutant strains, eye3-2 and ptx1, exhibit normal chemotaxis. This suggests that Chlamydomonas transduces the light signal pathway in chemotaxis differently from that in phototaxis. Second, we found that Chlamydomonas collectively migrate during chemotaxis but not phototaxis. Collective migration during chemotaxis is not clearly observed when the assay is conducted in the dark. Third, the Chlamydomonas strain CC-124 carrying agg1, the AGGREGATE1 gene (AGG1) null mutation, exhibited a more robust collective migratory response than strains carrying the wild-type AGG1 gene. The expression of a recombinant AGG1 protein in the CC-124 strain suppressed this collective migration during chemotaxis. Altogether, these findings suggest a unique mechanism; ammonium chemotaxis in Chlamydomonas is mainly driven by collective cell migration. Furthermore, it is proposed that collective migration is enhanced by light and suppressed by the AGG1 protein.

摘要

与调控光趋性的机制相比,莱茵衣藻的化学趋性调控机制在很大程度上尚不清楚,尽管在纤毛微藻的迁移反应中具有同等重要性。为了研究化学趋性,我们对传统的 Petri 盘测定法进行了简单的修改。利用该测定法,揭示了一种控制莱茵衣藻铵化学趋性的新机制。首先,我们发现光照增强了野生型莱茵衣藻菌株的趋化反应,但光趋性缺陷突变株 eye3-2 和 ptx1 表现出正常的趋化性。这表明,莱茵衣藻在趋化作用中传递光信号的途径与在光趋性中不同。其次,我们发现莱茵衣藻在趋化作用中集体迁移,但在光趋性中不集体迁移。在黑暗中进行测定时,趋化性过程中没有明显观察到集体迁移。第三,携带 agg1(AGGREGATE1 基因,AGG1)缺失突变的 CC-124 菌株比携带野生型 AGG1 基因的菌株表现出更强的集体迁移反应。在 CC-124 菌株中表达重组 AGG1 蛋白抑制了趋化性过程中的这种集体迁移。总之,这些发现表明了一种独特的机制;莱茵衣藻的铵趋化性主要由细胞集体迁移驱动。此外,据推测,集体迁移受光增强,受 AGG1 蛋白抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0fe/10319813/635211226b2c/41598_2023_36818_Fig1_HTML.jpg

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