دورية أكاديمية

Immunofluorescence staining of chloroplast proteins with frozen sections of plant tissues.

التفاصيل البيبلوغرافية
العنوان: Immunofluorescence staining of chloroplast proteins with frozen sections of plant tissues.
المؤلفون: Wang L; National Engineering Research Center of Tree Breeding and Ecological Restoration and State Key Laboratory of Efficient Production of Forest Resources, College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China., Zeng F; National Engineering Research Center of Tree Breeding and Ecological Restoration and State Key Laboratory of Efficient Production of Forest Resources, College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China., Jiao Y; National Engineering Research Center of Tree Breeding and Ecological Restoration and State Key Laboratory of Efficient Production of Forest Resources, College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China., Zhou Q; National Engineering Research Center of Tree Breeding and Ecological Restoration and State Key Laboratory of Efficient Production of Forest Resources, College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China., An J; National Engineering Research Center of Tree Breeding and Ecological Restoration and State Key Laboratory of Efficient Production of Forest Resources, College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China., Gao H; National Engineering Research Center of Tree Breeding and Ecological Restoration and State Key Laboratory of Efficient Production of Forest Resources, College of Biological Sciences and Technology, Beijing Forestry University, Beijing, 100083, China. gaohongbo@bjfu.edu.cn.
المصدر: Plant cell reports [Plant Cell Rep] 2024 Jun 12; Vol. 43 (7), pp. 168. Date of Electronic Publication: 2024 Jun 12.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Springer Country of Publication: Germany NLM ID: 9880970 Publication Model: Electronic Cited Medium: Internet ISSN: 1432-203X (Electronic) Linking ISSN: 07217714 NLM ISO Abbreviation: Plant Cell Rep Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Berlin ; New York : Springer, 1981-
مواضيع طبية MeSH: Arabidopsis*/metabolism , Arabidopsis*/cytology , Frozen Sections*/methods , Fluorescent Antibody Technique*/methods , Chloroplasts*/metabolism , Staining and Labeling*/methods , Chloroplast Proteins*/metabolism , Chloroplast Proteins*/genetics, Plant Leaves/metabolism ; Plant Leaves/cytology ; Arabidopsis Proteins/metabolism ; Arabidopsis Proteins/genetics ; Mesophyll Cells/metabolism ; Mesophyll Cells/cytology
مستخلص: Key Message: Immunofluorescence staining with frozen sections of plant tissues and a nest tube is convenient and effective, and broadens the applicability of immunofluorescence staining. Immunofluorescence staining is an indispensable and extensively employed technique for determining the subcellular localization of chloroplast division proteins. At present, it is difficult to effectively observe the localization of target proteins in leaves that are hard, or very thin, or have epidermal hair or glands with the current immunofluorescence staining methods. Moreover, signals of target proteins were predominantly detected in mesophyll cells, not the cells of other types. Thus, the method of immunofluorescence staining was further explored for improvement in this study. The plant tissue was embedded with 50% PEG4000 at -60℃, which was then cut into sections by a cryomacrotome. The sections were immediately immersed in fixation solution. Then, the sample was transferred into a special nested plastic tube, which facilitated the fixation and immunofluorescence staining procedures. The use of frozen sections in this method enabled a short processing time and reduced material requirements. By optimizing the thickness of the sections, a large proportion of the cells could be well stained. With this method, we observed the localization of a chloroplast division protein FtsZ1 in the wild-type Arabidopsis and various chloroplast division mutants. Meanwhile, the localization of FtsZ1 was also observed not only in mesophyll cells, but also in guard cells and epidermal cells in a lot of other plant species, including many species with hard leaf tissues. This method is not only easy to use, but also expands the scope of applicability for immunofluorescence staining.
(© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
References: Chang N, Gao Y, Zhao L, Liu X, Gao H (2015) Arabidopsis FHY3/CPD45 regulates far-red light signaling and chloroplast division in parallel. Sci Rep 5:9612. (PMID: 10.1038/srep09612258726424397536)
Chang N, Sun Q, Li Y, Mu Y, Hu J, Feng Y, Liu X, Gao H (2017) PDV2 has a dosage effect on chloroplast division in Arabidopsis. Plant Cell Rep 36:471–480. (PMID: 10.1007/s00299-016-2096-627988788)
Chen C, MacCready JS, Ducat DC, Osteryoung KW (2018) The molecular machinery of chloroplast division. Plant Physiol 176:138–151. (PMID: 10.1104/pp.17.0127229079653)
Chen C, Cao L, Yang Y, Porter KJ, Osteryoung KW (2019) ARC3 Activation by PARC6 promotes FtsZ-ring remodeling at the chloroplast division site. Plant Cell 31:862–885. (PMID: 10.1105/tpc.18.00948308245056501610)
Gao Y, Liu H, An C, Shi Y, Liu X, Yuan W, Zhang B, Yang J, Yu C, Gao H (2013) Arabidopsis FRS4/CPD25 and FHY3/CPD45 work cooperatively to promote the expression of the chloroplast division gene ARC5 and chloroplast division. The Plant Journal : for Cell and Molecular Biology 75:795–807. (PMID: 10.1111/tpj.1224023662592)
Hanson DA, Ziegler SF (2004) Fusion of green fluorescent protein to the C-terminus of granulysin alters its intracellular localization in comparison to the native molecule. J Negat Results Biomed 3:2. (PMID: 10.1186/1477-5751-3-215361253517947)
Li Y, Sun Q, Feng Y, Liu X, Gao H (2016) An improved immunofluorescence staining method for chloroplast proteins. Plant Cell Rep 35:2285–2293. (PMID: 10.1007/s00299-016-2034-727473527)
Liu X, An J, Wang L, Sun Q, An C, Wu B, Hong C, Wang X, Dong S, Guo J, Feng Y, Gao H (2022) A novel amphiphilic motif at the C-terminus of FtsZ1 facilitates chloroplast division. Plant Cell 34:419–432. (PMID: 10.1093/plcell/koab27234755875)
Miyagishima SY, Froehlich JE, Osteryoung KW (2006) PDV1 and PDV2 mediate recruitment of the dynamin-related protein ARC5 to the plastid division site. Plant Cell 18:2517–2530. (PMID: 10.1105/tpc.106.045484169980691626610)
Osteryoung KW, McAndrew RS (2001) The plastid division machine. Annu Rev Plant Physiol Plant Mol Biol 52:315–333. (PMID: 10.1146/annurev.arplant.52.1.31511337401)
Osteryoung KW, Nunnari J (2003) The division of endosymbiotic organelles. Science (new York, NY) 302:1698–1704. (PMID: 10.1126/science.1082192)
Osteryoung KW, Pyke KA (2014) Division and dynamic morphology of plastids. Annu Rev Plant Biol 65:443–472. (PMID: 10.1146/annurev-arplant-050213-03574824471836)
Ovečka M, Samajová O, Baluška F, Samaj J (2014) Immunofluorescent localization of MAPKs in Steedman’s wax sections. Methods in Molecular Biology (clifton, NJ) 1171:117–130. (PMID: 10.1007/978-1-4939-0922-3_10)
Pasternak T, Tietz O, Rapp K, Begheldo M, Nitschke R, Ruperti B, Palme K (2015) Protocol: an improved and universal procedure for whole-mount immunolocalization in plants. Plant Methods 11:50. (PMID: 10.1186/s13007-015-0094-2265163414625903)
Pyke KA, Leech RM (1994) A genetic analysis of chloroplast division and expansion in arabidopsis thaliana. Plant Physiol 104:201–207. (PMID: 10.1104/pp.104.1.20112232072159178)
Stokes KD, Osteryoung KW (2003) Early divergence of the FtsZ1 and FtsZ2 plastid division gene families in photosynthetic eukaryotes. Gene 320:97–108. (PMID: 10.1016/S0378-1119(03)00814-X14597393)
Sun Q, Cao X, Liu Z, An C, Hu J, Wang Y, Qiao M, Gao T, Cheng W, Zhang Y, Feng Y, Gao H (2023) Structural and functional insights into the chloroplast division site regulators PARC6 and PDV1 in the intermembrane space. Proc Natl Acad Sci USA 120:e2215575120. (PMID: 10.1073/pnas.2215575120366964459945983)
Vitha S, McAndrew RS, Osteryoung KW (2001) FtsZ ring formation at the chloroplast division site in plants. J Cell Biol 153:111–120. (PMID: 10.1083/jcb.153.1.111112852782185535)
Wang W, Li J, Sun Q, Yu X, Zhang W, Jia N, An C, Li Y, Dong Y, Han F, Chang N, Liu X, Zhu Z, Yu Y, Fan S, Yang M, Luo SZ, Gao H, Feng Y (2017) Structural insights into the coordination of plastid division by the ARC6-PDV2 complex. Nature Plants 3:17011. (PMID: 10.1038/nplants.2017.1128248291)
Wang L, Tang M, Huang W, An J, Liu X, Gao H (2022) A tissue-chopping based immunofluorescence staining method for chloroplast proteins. Front Plant Sci 13:910569. (PMID: 10.3389/fpls.2022.910569356651849161302)
Wang L, Chen Y, Niu D, Tang M, An J, Xue S, Liu X, Gao H (2023) Improvements for Tissue-Chopping-Based Immunofluorescence Staining Method of Chloroplast Proteins. Plants (basel, Switzerland) 12(4):841. (PMID: 36840189)
معلومات مُعتمدة: 32070696 National Natural Science Foundation of China; 32370746 National Natural Science Foundation of China
فهرسة مساهمة: Keywords: Chloroplast proteins; Frozen sections; Immunofluorescence staining; Plant tissues; Subcellular localization
المشرفين على المادة: 0 (Chloroplast Proteins)
0 (Arabidopsis Proteins)
تواريخ الأحداث: Date Created: 20240612 Date Completed: 20240612 Latest Revision: 20240715
رمز التحديث: 20240715
DOI: 10.1007/s00299-024-03255-2
PMID: 38864883
قاعدة البيانات: MEDLINE
الوصف
تدمد:1432-203X
DOI:10.1007/s00299-024-03255-2