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玉米 C4 循环突变体叶片中叶肉-束鞘界面的加速重塑。

Accelerated remodeling of the mesophyll-bundle sheath interface in the maize C4 cycle mutant leaves.

机构信息

State Key Laboratory of Agrobiotechnology, Center for Cell and Developmental Biology, School of Life Sciences, The Chinese University of Hong Kong, Hong Kong, China.

State Key Laboratory of Crop Biology, College of Agronomic Sciences, Shandong Agricultural University, Tai'an, 271018, China.

出版信息

Sci Rep. 2022 Mar 23;12(1):5057. doi: 10.1038/s41598-022-09135-7.

DOI:10.1038/s41598-022-09135-7
PMID:35322159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8943126/
Abstract

C4 photosynthesis in the maize leaf involves the exchange of organic acids between mesophyll (M) and the bundle sheath (BS) cells. The transport is mediated by plasmodesmata embedded in the suberized cell wall. We examined the maize Kranz anatomy with a focus on the plasmodesmata and cell wall suberization with microscopy methods. In the young leaf zone where M and BS cells had indistinguishable proplastids, plasmodesmata were simple and no suberin was detected. In leaf zones where dimorphic chloroplasts were evident, the plasmodesma acquired sphincter and cytoplasmic sleeves, and suberin was discerned. These modifications were accompanied by a drop in symplastic dye mobility at the M-BS boundary. We compared the kinetics of chloroplast differentiation and the modifications in M-BS connectivity in ppdk and dct2 mutants where C4 cycle is affected. The rate of chloroplast diversification did not alter, but plasmodesma remodeling, symplastic transport inhibition, and cell wall suberization were observed from younger leaf zone in the mutants than in wild type. Our results indicate that inactivation of the C4 genes accelerated the changes in the M-BS interface, and the reduced permeability suggests that symplastic transport between M and BS could be regulated for normal operation of C4 cycle.

摘要

玉米叶片中的 C4 光合作用涉及到质体(M)和束鞘(BS)细胞之间有机酸的交换。这种运输是由嵌入在木质素化细胞壁中的胞间连丝介导的。我们使用显微镜方法研究了玉米的 Kranz 解剖结构,重点研究了胞间连丝和细胞壁木质素化。在年轻叶片区,M 和 BS 细胞的前质体没有区别,胞间连丝是简单的,没有检测到木质素。在明显存在二型叶绿体的叶片区,胞间连丝获得了括约肌和细胞质套,并且可以分辨出木质素。这些修饰伴随着 M-BS 边界处的胞质染料流动性下降。我们比较了 ppdk 和 dct2 突变体中 C4 循环受到影响时叶绿体分化和 M-BS 连接性修饰的动力学。叶绿体多样化的速度没有改变,但是在突变体中,比在野生型中更早地观察到胞间连丝重塑、胞质运输抑制和细胞壁木质素化。我们的结果表明,C4 基因的失活加速了 M-BS 界面的变化,而渗透性的降低表明 M 和 BS 之间的胞质运输可能受到调节,以正常运行 C4 循环。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9c/8943126/8e03a96bd048/41598_2022_9135_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9c/8943126/bdc935287ec9/41598_2022_9135_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9c/8943126/f5488dc72dc5/41598_2022_9135_Fig5_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9c/8943126/8e03a96bd048/41598_2022_9135_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9c/8943126/bdc935287ec9/41598_2022_9135_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9c/8943126/566e095d02af/41598_2022_9135_Fig2_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9c/8943126/46ea75df06f2/41598_2022_9135_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a9c/8943126/8e03a96bd048/41598_2022_9135_Fig7_HTML.jpg

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