Evidence map›Paper›PMID 32488507›Full record

ArticleMarine biotechnology (New York, N.Y.)2020

Comparative Gene Analysis Focused on Silica Cell Wall Formation: Identification of Diatom-Specific SET Domain Protein Methyltransferases.

Michiko Nemoto, Sayako Iwaki, Hisao Moriya, Yuki Monden, Takashi Tamura, Kenji Inagaki, Shigeki Mayama, Kiori Obuse

Erratum issuedAbstract readComparative Study
PubMed Publisher
In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. The Art of Exploring Diatom Biosilica Biomaterials: From Biofabrication Perspective.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Review
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Michiko NemotoGraduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan. mnemoto@okayama-u.ac.jp.ORCID http://orcid.org/0000-0003-0551-5284
Sayako IwakiGraduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Hisao MoriyaGraduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Yuki MondenGraduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Takashi TamuraGraduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Kenji InagakiGraduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.
Shigeki MayamaDepartment of Biology, Tokyo Gakugei University, Tokyo, 184-8511, Japan.
Kiori ObuseGraduate School of Environmental and Life Science, Okayama University, Okayama, 700-8530, Japan.

Funding

Asahi Glass Foundation (JP) Kenkyu-SyoreiMinistry of Education, Culture, Sports, Science and Technology 18K05818Ministry of Education, Culture, Sports, Science and Technology the Program to Disseminate Tenure Tracking System
6 · The paper itself

Abstract

Silica cell walls of diatoms have attracted attention as a source of nanostructured functional materials and have immense potential for a variety of applications. Previous studies of silica cell wall formation have identified numerous involved proteins, but most of these proteins are species-specific and are not conserved among diatoms. However, because the basic process of diatom cell wall formation is common to all diatom species, ubiquitous proteins and molecules will reveal the mechanisms of cell wall formation. In this study, we assembled de novo transcriptomes of three diatom species, Nitzschia palea, Achnanthes kuwaitensis, and Pseudoleyanella lunata, and compared protein-coding genes of five genome-sequenced diatom species. These analyses revealed a number of diatom-specific genes that encode putative endoplasmic reticulum-targeting proteins. Significant numbers of these proteins showed homology to silicanin-1, which is a conserved diatom protein that reportedly contributes to cell wall formation. These proteins also included a previously unrecognized SET domain protein methyltransferase family that may regulate functions of cell wall formation-related proteins and long-chain polyamines. Proteomic analysis of cell wall-associated proteins in N. palea identified a protein that is also encoded by one of the diatom-specific genes. Expression analysis showed that candidate genes were upregulated in response to silicon, suggesting that these genes play roles in silica cell wall formation. These candidate genes can facilitate further investigations of silica cell wall formation in diatoms.

Indexed as

TranscriptomeCell WallDiatomsProtein MethyltransferasesPR-SET DomainsSilicon DioxideProtein MethyltransferasesSilicon DioxideBiomineralizationDiatomProteomeSilicaTranscriptome

Identifiers

What OpenQuestion holds

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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 OpenQuestion graph.