Evidence map›Paper›PMID 25994087›Full record

ArticleProtoplasma2016

Biogenesis of protein bodies during legumin accumulation in developing olive (Olea europaea L.) seed.

Jose C Jimenez-Lopez, Agnieszka Zienkiewicz, Krzysztof Zienkiewicz, Juan D Alché, Maria I Rodríguez-García

Abstract read
PubMed Publisher
In one paragraph

Article in Protoplasma, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 22% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Morphological, Anatomical, and Phytochemical Studies ofInternational journal of molecular sciences · 2020
    Article
  3. Article
  4. Article
  5. Article
  6. Narrow-Leafed Lupin (Frontiers in plant science · 2016
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 3 countries.

Jose C Jimenez-LopezThe UWA Institute of Agriculture, The University of Western Australia, 35 Stirling Highway, Crawley, Perth, WA, 6009, Australia. jcjimenezl75@gmail.com.
Agnieszka ZienkiewiczDepartment of Biochemistry, Cell and Molecular Biology of Plants, Estación Experimental del Zaidín, National Council for Scientific Research (CSIC), Profesor Albareda 1, Granada, 18008, Spain.
Krzysztof ZienkiewiczDepartment of Biochemistry, Cell and Molecular Biology of Plants, Estación Experimental del Zaidín, National Council for Scientific Research (CSIC), Profesor Albareda 1, Granada, 18008, Spain.
Juan D AlchéDepartment of Biochemistry, Cell and Molecular Biology of Plants, Estación Experimental del Zaidín, National Council for Scientific Research (CSIC), Profesor Albareda 1, Granada, 18008, Spain.
Maria I Rodríguez-GarcíaDepartment of Biochemistry, Cell and Molecular Biology of Plants, Estación Experimental del Zaidín, National Council for Scientific Research (CSIC), Profesor Albareda 1, Granada, 18008, Spain. mariaisabel.rodriguez@eez.csic.es.
Estación Experimental del Zaidín · ESNicolaus Copernicus University · PLUniversity of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Much of our current knowledge about seed development and differentiation regarding reserves synthesis and accumulation come from monocot (cereals) plants. Studies in dicotyledonous seeds differentiation are limited to a few species and in oleaginous species are even scarcer despite their agronomic and economic importance. We examined the changes accompanying the differentiation of olive endosperm and cotyledon with a focus on protein bodies (PBs) biogenesis during legumin protein synthesis and accumulation, with the aim of getting insights and a better understanding of the PBs' formation process. Cotyledon and endosperm undergo differentiation during seed development, where an asynchronous time-course of protein synthesis, accumulation, and differential PB formation patterns was found in both tissues. At the end of seed maturation, a broad population of PBs, particularly in cotyledon cells, was distinguishable in terms of number per cell and morphometric and cytochemical features. Olive seed development is a tissue-dependent process characterized by differential rates of legumin accumulation and PB formation in the main tissues integrating seed. One of the main features of the impressive differentiation process is the specific formation of a broad group of PBs, particularly in cotyledon cells, which might depend on selective accumulation and packaging of proteins and specific polypeptides into PBs. The nature and availability of the major components detected in the PBs of olive seed are key parameters in order to consider the potential use of this material as a suitable source of carbon and nitrogen for animal or even human use.

Indexed as

CotyledonEndospermLeguminsOleaPlant ProteinsLeguminsPlant ProteinsCotyledonDevelopmentEndospermLeguminProtein bodySeed

Identifiers

PMID25994087
OpenAlexW314448764

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.