Evidence map›Paper›PMID 41622174›Full record

ArticlePlant methods2026

Establishment of fluorescent protein-tagged lines for investigating dynamic localization of organelle and other cell structures in rice pollen tube.

Su-Kyoung Lee, Woo-Jong Hong, Eui-Jung Kim, Eun Young Kim, Ki-Hong Jung

Abstract read
In one paragraph

Article in Plant methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Su-Kyoung Lee *Graduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin, 17104, Republic of Korea.
Woo-Jong Hong *Graduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin, 17104, Republic of Korea.
Eui-Jung KimGraduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin, 17104, Republic of Korea.
Eun Young KimDepartment of Smart Farm Science, Kyung Hee University, Yongin, 17104, Republic of Korea.
Ki-Hong JungGraduate School of Green-Bio Science & Crop Biotech Institute, Kyung Hee University, Yongin, 17104, Republic of Korea. khjung2010@khu.ac.kr.

Funding

National Research Foundation of Korea RS-2021-NR059380National Research Foundation of Korea RS-2021-NR062086
6 · The paper itself

Abstract

Eukaryotic cells consist of various organelles, each responsible for specific biological processes, making the understanding of protein subcellular localization essential for determining their potential functions. However, the rapid polar growth of pollen tubes requires careful consideration of organelle trafficking when analyzing subcellular localization in related studies. Fluorescence-tagged organelle markers have shown limited utility for studying pollen during the reproductive stage. In this study, we developed pollen-specific fluorescent marker sets for organelles and other cell structures using the promoter of the OsTAPE gene, which is highly expressed in mature pollen and pollen tubes of rice (Oryza sativa L.). These marker sets enable the visualization of cell membranes, nuclei, endoplasmic reticulum, Golgi apparatus, prevacuolar compartments, and filamentous actin by tagging fluorescent proteins (FP) at the amino N-terminal end. Specifically designed to accommodate the rapid tube elongation of rice pollen, this system offers a valuable resource for gene function research and colocalization analysis, helping to elucidate the pollen tube elongation process. This study expands the potential for using fluorescent labeling in monocotyledonous plants like rice during reproductive stages, facilitating gene function studies under varying environmental conditions through subcellular localization analysis in growing pollen tubes.

Indexed as

Cell structureMarker lineOrganelleOryza sativaPollen tube

Identifiers

PMID41622174
PMCPMC12952121

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