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C4光合作用的进化趋同:紫茉莉科的一个案例研究

Evolutionary Convergence of C Photosynthesis: A Case Study in the Nyctaginaceae.

作者信息

Khoshravesh Roxana, Stata Matt, Adachi Shunsuke, Sage Tammy L, Sage Rowan F

机构信息

Department of Ecology and Evolutionary Biology, The University of Toronto, Toronto, ON, Canada.

Department of Biology, The University of New Mexico, Albuquerque, NM, United States.

出版信息

Front Plant Sci. 2020 Nov 2;11:578739. doi: 10.3389/fpls.2020.578739. eCollection 2020.

Abstract

C photosynthesis evolved over 65 times, with around 24 origins in the eudicot order Caryophyllales. In the Caryophyllales family Nyctaginaceae, the C pathway is known in three genera of the tribe Nyctagineae: , and Phylogenetically, and are separated by three genera whose photosynthetic pathway is uncertain. To clarify the distribution of photosynthetic pathways in the Nyctaginaceae, we surveyed carbon isotope ratios of 159 species of the Nyctaginaceae, along with bundle sheath (BS) cell ultrastructure, leaf gas exchange, and C pathway biochemistry in five species from the two C clades and closely related C genera. All species in and are C, while no C species occur in any other genera of the family, including three that branch between and . This demonstrates that C photosynthesis evolved twice in Nyctaginaceae. species use the NADP-malic enzyme (NADP-ME) subtype of C photosynthesis, while species use the NAD-malic enzyme (NAD-ME) subtype. The BS cells of have many more mitochondria than the BS of . Bundle sheath mitochondria are closely associated with chloroplasts in which facilitates CO refixation following decarboxylation by mitochondrial NAD-ME. The close relationship between and could provide insights into why NADP-ME versus NAD-ME subtypes evolve, particularly when coupled to analysis of their respective genomes. As such, the group is an excellent system to dissect the organizational hierarchy of convergent versus divergent traits produced by C evolution, enabling us to understand when convergence is favored versus when divergent modifications can result in a common phenotype.

摘要

C4光合作用独立进化了65次以上,在真双子叶植物石竹目约有24次起源。在紫茉莉科紫茉莉族中,已知有三个属具有C4途径:紫茉莉属、叶子花属和腺果藤属。在系统发育上,紫茉莉属和叶子花属被三个光合途径不确定的属隔开。为了阐明紫茉莉科光合途径的分布,我们调查了紫茉莉科159个物种的碳同位素比率,以及来自两个C4分支和与之密切相关的C3属的五个物种的维管束鞘(BS)细胞超微结构、叶片气体交换和C4途径生物化学。紫茉莉属和叶子花属的所有物种都是C4植物,而该科的任何其他属都没有C4物种,包括在紫茉莉属和叶子花属之间分支的三个属。这表明C4光合作用在紫茉莉科中独立进化了两次。紫茉莉属物种使用C4光合作用的NADP-苹果酸酶(NADP-ME)亚型,而叶子花属物种使用NAD-苹果酸酶(NAD-ME)亚型。叶子花属的维管束鞘细胞比紫茉莉属的维管束鞘细胞有更多的线粒体。在叶子花属中,维管束鞘线粒体与叶绿体紧密相连,这有助于线粒体NAD-ME脱羧后CO2的再固定。紫茉莉属和叶子花属之间的密切关系可以为为什么会进化出NADP-ME与NAD-ME亚型提供见解,特别是当与它们各自基因组的分析相结合时。因此,该类群是一个很好的系统,用于剖析C4进化产生的趋同与趋异性状的组织层次结构,使我们能够了解何时趋同更有利,以及何时趋异修饰会导致共同的表型。

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