Loading…

Electron tomography of prolamellar bodies and their transformation into grana thylakoids in cryofixed Arabidopsis cotyledons

The para-crystalline structures of prolamellar bodies (PLBs) and light-induced etioplast-to-chloroplast transformation have been investigated via electron microscopy. However, such studies suffer from chemical fixation artifacts and limited volumes of 3D reconstruction. Here, we examined Arabidopsis...

Full description

Saved in:
Bibliographic Details
Published in:The Plant cell 2022-09, Vol.34 (10), p.3830-3843
Main Authors: Liang, Zizhen, Yeung, Wai-Tsun, Ma, Juncai, Mai, Keith Ka Ki, Liu, Zhongyuan, Chong, Yau-Lun Felix, Cai, Xiaohao, Kang, Byung-Ho
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c390t-a69e66d170af24be14070269d755376ce50b7d4819f66c9cb17cb207e8b3ecb83
cites cdi_FETCH-LOGICAL-c390t-a69e66d170af24be14070269d755376ce50b7d4819f66c9cb17cb207e8b3ecb83
container_end_page 3843
container_issue 10
container_start_page 3830
container_title The Plant cell
container_volume 34
creator Liang, Zizhen
Yeung, Wai-Tsun
Ma, Juncai
Mai, Keith Ka Ki
Liu, Zhongyuan
Chong, Yau-Lun Felix
Cai, Xiaohao
Kang, Byung-Ho
description The para-crystalline structures of prolamellar bodies (PLBs) and light-induced etioplast-to-chloroplast transformation have been investigated via electron microscopy. However, such studies suffer from chemical fixation artifacts and limited volumes of 3D reconstruction. Here, we examined Arabidopsis thaliana cotyledon cells by electron tomography (ET) to visualize etioplasts and their conversion into chloroplasts. We employed scanning transmission ET to image large volumes and high-pressure freezing to improve sample preservation. PLB tubules were arranged in a zinc blende-type lattice-like carbon atoms in diamonds. Within 2 h after illumination, the lattice collapsed from the PLB exterior and the disorganized tubules merged to form thylakoid sheets (pre-granal thylakoids), which folded and overlapped with each other to create grana stacks. Since the nascent pre-granal thylakoids contained curved membranes in their tips, we examined the expression and localization of CURT1 (CURVATURE THYLAKOID1) proteins. CURT1A transcripts were most abundant in de-etiolating cotyledon samples, and CURT1A was concentrated at the PLB periphery. In curt1a etioplasts, PLB-associated thylakoids were swollen and failed to form grana stacks. In contrast, PLBs had cracks in their lattices in curt1c etioplasts. Our data provide evidence that CURT1A is required for pre-granal thylakoid assembly from PLB tubules during de-etiolation, while CURT1C contributes to cubic crystal growth in the dark.
doi_str_mv 10.1093/plcell/koac205
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9516191</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2694415600</sourcerecordid><originalsourceid>FETCH-LOGICAL-c390t-a69e66d170af24be14070269d755376ce50b7d4819f66c9cb17cb207e8b3ecb83</originalsourceid><addsrcrecordid>eNpVUU1rFTEUDaLYWt26lCzdTJvMTJLJRiiltkLBjYK7kK_pi83kjkmeOOCPN-U9i67u5d5zzv04CL2l5JwSOVys0foYLx5A256wZ-iUsqHvejl9e95yMpJu5IyeoFelfCeEUEHlS3QysEnwifJT9Ps6elszJFxhgfus192GYcZrhqiXJq0zNuCCL1gnh-vOh4xr1qnMkBddQ2OGVAE3atKtv0X9AMGVVsU2bzCHX97hy6xNcLCWULCFukXvIJXX6MWsY_FvjvEMff14_eXqtrv7fPPp6vKus4MktdNces4dFUTP_Wg8HYkgPZdOMDYIbj0jRrhxonLm3EprqLCmJ8JPZvDWTMMZ-nDQXfdm8c761C6Ias1h0XlToIP6v5PCTt3DTyUZ5VTSJvD-KJDhx96XqpZQHh-vk4d9UW2ZcaSME9Kg5weozVBK9vPTGErUo2XqYJk6WtYI7_5d7gn-16PhDyLGmbY</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2694415600</pqid></control><display><type>article</type><title>Electron tomography of prolamellar bodies and their transformation into grana thylakoids in cryofixed Arabidopsis cotyledons</title><source>Oxford Journals Online</source><creator>Liang, Zizhen ; Yeung, Wai-Tsun ; Ma, Juncai ; Mai, Keith Ka Ki ; Liu, Zhongyuan ; Chong, Yau-Lun Felix ; Cai, Xiaohao ; Kang, Byung-Ho</creator><creatorcontrib>Liang, Zizhen ; Yeung, Wai-Tsun ; Ma, Juncai ; Mai, Keith Ka Ki ; Liu, Zhongyuan ; Chong, Yau-Lun Felix ; Cai, Xiaohao ; Kang, Byung-Ho</creatorcontrib><description>The para-crystalline structures of prolamellar bodies (PLBs) and light-induced etioplast-to-chloroplast transformation have been investigated via electron microscopy. However, such studies suffer from chemical fixation artifacts and limited volumes of 3D reconstruction. Here, we examined Arabidopsis thaliana cotyledon cells by electron tomography (ET) to visualize etioplasts and their conversion into chloroplasts. We employed scanning transmission ET to image large volumes and high-pressure freezing to improve sample preservation. PLB tubules were arranged in a zinc blende-type lattice-like carbon atoms in diamonds. Within 2 h after illumination, the lattice collapsed from the PLB exterior and the disorganized tubules merged to form thylakoid sheets (pre-granal thylakoids), which folded and overlapped with each other to create grana stacks. Since the nascent pre-granal thylakoids contained curved membranes in their tips, we examined the expression and localization of CURT1 (CURVATURE THYLAKOID1) proteins. CURT1A transcripts were most abundant in de-etiolating cotyledon samples, and CURT1A was concentrated at the PLB periphery. In curt1a etioplasts, PLB-associated thylakoids were swollen and failed to form grana stacks. In contrast, PLBs had cracks in their lattices in curt1c etioplasts. Our data provide evidence that CURT1A is required for pre-granal thylakoid assembly from PLB tubules during de-etiolation, while CURT1C contributes to cubic crystal growth in the dark.</description><identifier>ISSN: 1040-4651</identifier><identifier>EISSN: 1532-298X</identifier><identifier>DOI: 10.1093/plcell/koac205</identifier><identifier>PMID: 35876816</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Arabidopsis - genetics ; Arabidopsis - metabolism ; Carbon - metabolism ; Chloroplasts - metabolism ; Cotyledon ; Diamond - analysis ; Diamond - metabolism ; Electron Microscope Tomography ; Thylakoids - metabolism ; Zinc - metabolism</subject><ispartof>The Plant cell, 2022-09, Vol.34 (10), p.3830-3843</ispartof><rights>American Society of Plant Biologists 2022. All rights reserved. For permissions, please email: journals.permissions@oup.com.</rights><rights>American Society of Plant Biologists 2022. All rights reserved. For permissions, please email: journals.permissions@oup.com 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-a69e66d170af24be14070269d755376ce50b7d4819f66c9cb17cb207e8b3ecb83</citedby><cites>FETCH-LOGICAL-c390t-a69e66d170af24be14070269d755376ce50b7d4819f66c9cb17cb207e8b3ecb83</cites><orcidid>0000-0003-3679-3842 ; 0000-0002-8622-0674 ; 0000-0002-0264-7807 ; 0000-0003-0924-2834 ; 0000-0002-5693-1117 ; 0000-0001-9283-0383 ; 0000-0002-4996-6709 ; 0000-0002-4299-2170</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35876816$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liang, Zizhen</creatorcontrib><creatorcontrib>Yeung, Wai-Tsun</creatorcontrib><creatorcontrib>Ma, Juncai</creatorcontrib><creatorcontrib>Mai, Keith Ka Ki</creatorcontrib><creatorcontrib>Liu, Zhongyuan</creatorcontrib><creatorcontrib>Chong, Yau-Lun Felix</creatorcontrib><creatorcontrib>Cai, Xiaohao</creatorcontrib><creatorcontrib>Kang, Byung-Ho</creatorcontrib><title>Electron tomography of prolamellar bodies and their transformation into grana thylakoids in cryofixed Arabidopsis cotyledons</title><title>The Plant cell</title><addtitle>Plant Cell</addtitle><description>The para-crystalline structures of prolamellar bodies (PLBs) and light-induced etioplast-to-chloroplast transformation have been investigated via electron microscopy. However, such studies suffer from chemical fixation artifacts and limited volumes of 3D reconstruction. Here, we examined Arabidopsis thaliana cotyledon cells by electron tomography (ET) to visualize etioplasts and their conversion into chloroplasts. We employed scanning transmission ET to image large volumes and high-pressure freezing to improve sample preservation. PLB tubules were arranged in a zinc blende-type lattice-like carbon atoms in diamonds. Within 2 h after illumination, the lattice collapsed from the PLB exterior and the disorganized tubules merged to form thylakoid sheets (pre-granal thylakoids), which folded and overlapped with each other to create grana stacks. Since the nascent pre-granal thylakoids contained curved membranes in their tips, we examined the expression and localization of CURT1 (CURVATURE THYLAKOID1) proteins. CURT1A transcripts were most abundant in de-etiolating cotyledon samples, and CURT1A was concentrated at the PLB periphery. In curt1a etioplasts, PLB-associated thylakoids were swollen and failed to form grana stacks. In contrast, PLBs had cracks in their lattices in curt1c etioplasts. Our data provide evidence that CURT1A is required for pre-granal thylakoid assembly from PLB tubules during de-etiolation, while CURT1C contributes to cubic crystal growth in the dark.</description><subject>Arabidopsis - genetics</subject><subject>Arabidopsis - metabolism</subject><subject>Carbon - metabolism</subject><subject>Chloroplasts - metabolism</subject><subject>Cotyledon</subject><subject>Diamond - analysis</subject><subject>Diamond - metabolism</subject><subject>Electron Microscope Tomography</subject><subject>Thylakoids - metabolism</subject><subject>Zinc - metabolism</subject><issn>1040-4651</issn><issn>1532-298X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpVUU1rFTEUDaLYWt26lCzdTJvMTJLJRiiltkLBjYK7kK_pi83kjkmeOOCPN-U9i67u5d5zzv04CL2l5JwSOVys0foYLx5A256wZ-iUsqHvejl9e95yMpJu5IyeoFelfCeEUEHlS3QysEnwifJT9Ps6elszJFxhgfus192GYcZrhqiXJq0zNuCCL1gnh-vOh4xr1qnMkBddQ2OGVAE3atKtv0X9AMGVVsU2bzCHX97hy6xNcLCWULCFukXvIJXX6MWsY_FvjvEMff14_eXqtrv7fPPp6vKus4MktdNces4dFUTP_Wg8HYkgPZdOMDYIbj0jRrhxonLm3EprqLCmJ8JPZvDWTMMZ-nDQXfdm8c761C6Ias1h0XlToIP6v5PCTt3DTyUZ5VTSJvD-KJDhx96XqpZQHh-vk4d9UW2ZcaSME9Kg5weozVBK9vPTGErUo2XqYJk6WtYI7_5d7gn-16PhDyLGmbY</recordid><startdate>20220927</startdate><enddate>20220927</enddate><creator>Liang, Zizhen</creator><creator>Yeung, Wai-Tsun</creator><creator>Ma, Juncai</creator><creator>Mai, Keith Ka Ki</creator><creator>Liu, Zhongyuan</creator><creator>Chong, Yau-Lun Felix</creator><creator>Cai, Xiaohao</creator><creator>Kang, Byung-Ho</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-3679-3842</orcidid><orcidid>https://orcid.org/0000-0002-8622-0674</orcidid><orcidid>https://orcid.org/0000-0002-0264-7807</orcidid><orcidid>https://orcid.org/0000-0003-0924-2834</orcidid><orcidid>https://orcid.org/0000-0002-5693-1117</orcidid><orcidid>https://orcid.org/0000-0001-9283-0383</orcidid><orcidid>https://orcid.org/0000-0002-4996-6709</orcidid><orcidid>https://orcid.org/0000-0002-4299-2170</orcidid></search><sort><creationdate>20220927</creationdate><title>Electron tomography of prolamellar bodies and their transformation into grana thylakoids in cryofixed Arabidopsis cotyledons</title><author>Liang, Zizhen ; Yeung, Wai-Tsun ; Ma, Juncai ; Mai, Keith Ka Ki ; Liu, Zhongyuan ; Chong, Yau-Lun Felix ; Cai, Xiaohao ; Kang, Byung-Ho</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-a69e66d170af24be14070269d755376ce50b7d4819f66c9cb17cb207e8b3ecb83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Arabidopsis - genetics</topic><topic>Arabidopsis - metabolism</topic><topic>Carbon - metabolism</topic><topic>Chloroplasts - metabolism</topic><topic>Cotyledon</topic><topic>Diamond - analysis</topic><topic>Diamond - metabolism</topic><topic>Electron Microscope Tomography</topic><topic>Thylakoids - metabolism</topic><topic>Zinc - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liang, Zizhen</creatorcontrib><creatorcontrib>Yeung, Wai-Tsun</creatorcontrib><creatorcontrib>Ma, Juncai</creatorcontrib><creatorcontrib>Mai, Keith Ka Ki</creatorcontrib><creatorcontrib>Liu, Zhongyuan</creatorcontrib><creatorcontrib>Chong, Yau-Lun Felix</creatorcontrib><creatorcontrib>Cai, Xiaohao</creatorcontrib><creatorcontrib>Kang, Byung-Ho</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Plant cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liang, Zizhen</au><au>Yeung, Wai-Tsun</au><au>Ma, Juncai</au><au>Mai, Keith Ka Ki</au><au>Liu, Zhongyuan</au><au>Chong, Yau-Lun Felix</au><au>Cai, Xiaohao</au><au>Kang, Byung-Ho</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electron tomography of prolamellar bodies and their transformation into grana thylakoids in cryofixed Arabidopsis cotyledons</atitle><jtitle>The Plant cell</jtitle><addtitle>Plant Cell</addtitle><date>2022-09-27</date><risdate>2022</risdate><volume>34</volume><issue>10</issue><spage>3830</spage><epage>3843</epage><pages>3830-3843</pages><issn>1040-4651</issn><eissn>1532-298X</eissn><abstract>The para-crystalline structures of prolamellar bodies (PLBs) and light-induced etioplast-to-chloroplast transformation have been investigated via electron microscopy. However, such studies suffer from chemical fixation artifacts and limited volumes of 3D reconstruction. Here, we examined Arabidopsis thaliana cotyledon cells by electron tomography (ET) to visualize etioplasts and their conversion into chloroplasts. We employed scanning transmission ET to image large volumes and high-pressure freezing to improve sample preservation. PLB tubules were arranged in a zinc blende-type lattice-like carbon atoms in diamonds. Within 2 h after illumination, the lattice collapsed from the PLB exterior and the disorganized tubules merged to form thylakoid sheets (pre-granal thylakoids), which folded and overlapped with each other to create grana stacks. Since the nascent pre-granal thylakoids contained curved membranes in their tips, we examined the expression and localization of CURT1 (CURVATURE THYLAKOID1) proteins. CURT1A transcripts were most abundant in de-etiolating cotyledon samples, and CURT1A was concentrated at the PLB periphery. In curt1a etioplasts, PLB-associated thylakoids were swollen and failed to form grana stacks. In contrast, PLBs had cracks in their lattices in curt1c etioplasts. Our data provide evidence that CURT1A is required for pre-granal thylakoid assembly from PLB tubules during de-etiolation, while CURT1C contributes to cubic crystal growth in the dark.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>35876816</pmid><doi>10.1093/plcell/koac205</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-3679-3842</orcidid><orcidid>https://orcid.org/0000-0002-8622-0674</orcidid><orcidid>https://orcid.org/0000-0002-0264-7807</orcidid><orcidid>https://orcid.org/0000-0003-0924-2834</orcidid><orcidid>https://orcid.org/0000-0002-5693-1117</orcidid><orcidid>https://orcid.org/0000-0001-9283-0383</orcidid><orcidid>https://orcid.org/0000-0002-4996-6709</orcidid><orcidid>https://orcid.org/0000-0002-4299-2170</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1040-4651
ispartof The Plant cell, 2022-09, Vol.34 (10), p.3830-3843
issn 1040-4651
1532-298X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9516191
source Oxford Journals Online
subjects Arabidopsis - genetics
Arabidopsis - metabolism
Carbon - metabolism
Chloroplasts - metabolism
Cotyledon
Diamond - analysis
Diamond - metabolism
Electron Microscope Tomography
Thylakoids - metabolism
Zinc - metabolism
title Electron tomography of prolamellar bodies and their transformation into grana thylakoids in cryofixed Arabidopsis cotyledons
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T04%3A27%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Electron%20tomography%20of%20prolamellar%20bodies%20and%20their%20transformation%20into%20grana%20thylakoids%20in%20cryofixed%20Arabidopsis%20cotyledons&rft.jtitle=The%20Plant%20cell&rft.au=Liang,%20Zizhen&rft.date=2022-09-27&rft.volume=34&rft.issue=10&rft.spage=3830&rft.epage=3843&rft.pages=3830-3843&rft.issn=1040-4651&rft.eissn=1532-298X&rft_id=info:doi/10.1093/plcell/koac205&rft_dat=%3Cproquest_pubme%3E2694415600%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c390t-a69e66d170af24be14070269d755376ce50b7d4819f66c9cb17cb207e8b3ecb83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2694415600&rft_id=info:pmid/35876816&rfr_iscdi=true