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小立碗藓质体乙醇酸/甘油酸转运蛋白敲除系中丝状体细胞的弯曲

Bending of protonema cells in a plastid glycolate/glycerate transporter knockout line of Physcomitrella patens.

作者信息

Nakahara Jin, Takechi Katsuaki, Myouga Fumiyoshi, Moriyama Yasuko, Sato Hiroshi, Takio Susumu, Takano Hiroyoshi

机构信息

Graduate School of Science and Technology, Kumamoto University, Kurokami, Kumamoto 860-8555, Japan.

Gene Discovery Research Group, RIKEN Center for Sustainable Resource Science (CSRS), Yokohama, Kanagawa 230-0045, Japan.

出版信息

PLoS One. 2015 Mar 20;10(3):e0118804. doi: 10.1371/journal.pone.0118804. eCollection 2015.

Abstract

Arabidopsis LrgB (synonym PLGG1) is a plastid glycolate/glycerate transporter associated with recycling of 2-phosphoglycolate generated via the oxygenase activity of ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO). We isolated two homologous genes (PpLrgB1 and B2) from the moss Physcomitrella patens. Phylogenetic tree analysis showed that PpLrgB1 was monophyletic with LrgB proteins of land plants, whereas PpLrgB2 was divergent from the green plant lineage. Experiments with PpLrgB-GFP fusion proteins suggested that both PpLrgB1 and B2 proteins were located in chloroplasts. We generated PpLrgB single (∆B1 and ∆B2) and double (∆B1/∆B2)-knockout lines using gene targeting of P. patens. The ∆B1 plants showed decreases in growth and photosynthetic activity, and their protonema cells were bent and accumulated glycolate. However, because ∆B2 and ∆B1/∆B2 plants showed no obvious phenotypic change relative to the wild-type or ∆B1 plants, respectively, the function of PpLrgB2 remains unclear. Arabidopsis LrgB could complement the ∆B1 phenotype, suggesting that the function of PpLrgB1 is the same as that of AtLrgB. When ∆B1 was grown under high-CO2 conditions, all novel phenotypes were suppressed. Moreover, protonema cells of wild-type plants exhibited a bending phenotype when cultured on media containing glycolate or glycerate, suggesting that accumulation of photorespiratory metabolites caused P. patens cells to bend.

摘要

拟南芥LrgB(同义词PLGG1)是一种质体乙醇酸/甘油酸转运蛋白,与通过1,5-二磷酸核酮糖羧化酶/加氧酶(RuBisCO)的加氧酶活性产生的2-磷酸乙醇酸的回收利用相关。我们从苔藓小立碗藓中分离出两个同源基因(PpLrgB1和B2)。系统发育树分析表明,PpLrgB1与陆地植物的LrgB蛋白是单系的,而PpLrgB2与绿色植物谱系不同。对PpLrgB-GFP融合蛋白的实验表明,PpLrgB1和B2蛋白都位于叶绿体中。我们利用小立碗藓的基因靶向技术构建了PpLrgB单基因敲除株系(∆B1和∆B2)和双基因敲除株系(∆B1/∆B2)。∆B1植株的生长和光合活性降低,其原丝体细胞弯曲并积累乙醇酸。然而,由于∆B2和∆B1/∆B2植株分别相对于野生型或∆B1植株没有表现出明显的表型变化,PpLrgB2的功能仍不清楚。拟南芥LrgB可以互补∆B1的表型,这表明PpLrgB1的功能与AtLrgB相同。当∆B1在高二氧化碳条件下生长时,所有新的表型都受到抑制。此外,野生型植株的原丝体细胞在含有乙醇酸或甘油酸的培养基上培养时表现出弯曲表型,这表明光呼吸代谢产物的积累导致小立碗藓细胞弯曲。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fec4/4368765/8fe577e3f25c/pone.0118804.g001.jpg

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