Evidence map›Paper›PMID 21706447›Full record

ArticleDevelopment genes and evolution2011

HpSumf1 is involved in the activation of sulfatases responsible for regulation of skeletogenesis during sea urchin development.

Tetsushi Sakuma, Kazuya Ohnishi, Kazumasa Fujita, Hiroshi Ochiai, Naoaki Sakamoto, Takashi Yamamoto

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Article in Development genes and evolution, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 89% of its field
1 · What the graph read from it

What it found

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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

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Tetsushi SakumaDepartment of Mathematical and Life Sciences, Graduate School of Science, Hiroshima University, Japan.
Kazuya Ohnishi
Kazumasa Fujita
Hiroshi Ochiai
Naoaki Sakamoto
Takashi Yamamoto
Hiroshima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sulfatases such as arylsulfatase and heparan sulfate 6-O-endosulfatase play important roles in morphogenesis during sea urchin development. For the activation of these sulfatases, Cα-formylglycine formation by sulfatase modifying factor (Sumf) is required. In this study, to clarify the regulatory mechanisms for the activation of sulfatases during sea urchin development, we examined the expression and function of the Hemicentrotus pulcherrimus homologs of Sumf1 and Sumf2 (HpSumf1 and HpSumf2, respectively). Expression of HpSumf1 but not HpSumf2 mRNA was dynamically changed during early development. Functional analyses of recombinant HpSumf1 and HpSumf2 using HEK293T cells expressing mouse arylsulfatase A (ArsA) indicated that HpSumf1 and HpSumf2 were both able to activate mammalian ArsA. Knockdown of HpSumf1 using morpholino antisense oligonucleotides caused abnormal spicule formation in the sea urchin embryo. Injection of HpSumf2 mRNA had no effect on skeletogenesis, while injection of HpSumf1 mRNA induced severe supernumerary spicule formation. Taken together, these findings suggest that HpSumf1 is involved in the activation of sulfatases required for control of skeletogenesis.

Indexed as

SkeletonAmino Acid SequenceAnimalsCells, CulturedCerebroside-SulfataseCloning, MolecularEmbryo, NonmammalianEnzyme ActivationGene Expression Regulation, DevelopmentalHemicentrotusMiceMolecular Sequence DataOligonucleotides, AntisenseOxidoreductases Acting on Sulfur Group DonorsRecombinant ProteinsRNA, MessengerCerebroside-SulfataseOligonucleotides, AntisenseOxidoreductases Acting on Sulfur Group DonorsRecombinant ProteinsRNA, MessengerSulfatasesSumf1 protein, mouseSUMF2 protein, human

Identifiers

PMID21706447
OpenAlexW2032717959

What OpenQuestion holds

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Registered trials

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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.