Evidence map›Paper›PMID 27230618›Full record

ArticleMarine biotechnology (New York, N.Y.)2016

Characterization of an Alpha Type Carbonic Anhydrase from Paracentrotus lividus Sea Urchin Embryos.

Konstantinos Karakostis, Caterina Costa, Francesca Zito, Franz Brümmer, Valeria Matranga

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.3field-weighted citation impact, top 32% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Extracellular carbonic anhydrase activity promotes a carbon concentration mechanism in metazoan calcifying cells.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  3. Article
  4. Comparison of Carbonic Anhydrases for COInternational journal of molecular sciences · 2022
    Article
  5. Article
  6. Article
  7. Review
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 2 institutions in 2 countries.

Konstantinos KarakostisInstitute of Biomedicine and Molecular Immunology "A. Monroy", National Research Council, Via Ugo La Malfa, 153-90146, Palermo, Italy.
Caterina CostaInstitute of Biomedicine and Molecular Immunology "A. Monroy", National Research Council, Via Ugo La Malfa, 153-90146, Palermo, Italy. caterina.costa@ibim.cnr.it.
Francesca ZitoInstitute of Biomedicine and Molecular Immunology "A. Monroy", National Research Council, Via Ugo La Malfa, 153-90146, Palermo, Italy.
Franz BrümmerInstitute for Biomaterials and Biomolecular Systems, University of Stuttgart, Stuttgart, Germany.
Valeria MatrangaInstitute of Biomedicine and Molecular Immunology "A. Monroy", National Research Council, Via Ugo La Malfa, 153-90146, Palermo, Italy.
National Research Council · ITUniversity of Stuttgart · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carbonic anhydrases (CA) are zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide to bicarbonate. In the sea urchin, CA has a role in the formation of the calcitic skeleton during embryo development. Here, we report a newly identified mRNA sequence from embryos of the sea urchin Paracentrotus lividus, referred to as Pl-can. The complete coding sequence was identified with the aid of both EST databases and experimental procedures. Pl-CAN is a 447 aa-long protein, with an estimated molecular mass of 48.5 kDa and an isoelectric point of 6.83. The in silico study of functional domains showed, in addition to the alpha type CA-specific domain, the presence of an unexpected glycine-rich region at the N-terminal of the molecule. This is not found in any other species described so far, but probably it is restricted to the sea urchins. The phylogenetic analysis indicated that Pl-CAN is evolutionarily closer to human among chordates than to other species. The putative role(s) of the identified domains is discussed. The Pl-can temporal and spatial expression profiles, analyzed throughout embryo development by comparative qPCR and whole-mount in situ hybridization (WMISH), showed that Pl-can mRNA is specifically expressed in the primary mesenchyme cells (PMC) of the embryo and levels increase along with the growth of the embryonic skeleton, reaching a peak at the pluteus stage. A recombinant fusion protein was produced in E. coli and used to raise specific antibodies in mice recognized the endogenous Pl-CAN by Western blot in embryo extracts from gastrula and pluteus.

Indexed as

Gene Expression Regulation, DevelopmentalAmino Acid SequenceAnimalsCarbonic AnhydrasesCloning, MolecularDNA, ComplementaryEmbryo, NonmammalianEscherichia coliIsoelectric PointMolecular WeightOpen Reading FramesOrgan SpecificityParacentrotusPhylogenyProtein DomainsRecombinant Fusion ProteinsCarbonic AnhydrasesDNA, ComplementaryRecombinant Fusion ProteinsRNA, MessengerBiomineralizationDevelopmentGene expressionRecombinant proteinsSkeletogenesis

Identifiers

PMID27230618
OpenAlexW2398187779

What OpenQuestion 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 OpenQuestion graph.