Evidence map›Paper›PMID 2663877›Full record

ArticleThe Journal of cell biology1989

A calsequestrin-like protein in the endoplasmic reticulum of the sea urchin: localization and dynamics in the egg and first cell cycle embryo.

J H Henson, D A Begg, S M Beaulieu, D J Fishkind, E M Bonder, M Terasaki, D Lebeche, B Kaminer

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1989. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
9.0field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 102 citations in OpenAlex.

  1. Mitotic spindle membranes.Molecular biology of the cell · 2025
    Review
  2. Calsequestrin, a key protein in striated muscle health and disease.Journal of muscle research and cell motility · 2021
    Review
  3. Article
  4. Calcium signalling in early embryos.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2008
    Review
  5. Review
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  9. Calsequestrinlike calcium-binding protein is expressed in calcium-accumulating cells of Pistia stratiotes.Proceedings of the National Academy of Sciences of the United States of America · 1993
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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

8 authors at 1 institution in 1 country.

J H HensonDepartment of Anatomy and Cellular Biology, Harvard Medical School, Boston, Massachusetts 02115.
D A Begg
S M Beaulieu
D J Fishkind
E M Bonder
M Terasaki
D Lebeche
B Kaminer
Harvard University · US

Funding

REGULATION OF FERTILIZATION AND EARLY EMBRYOGENESISR01HD020140 · NICHD · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BEGG, DAVID A · 1987 to 1989
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ER IN EGG--CONSTITUENTS AND LOCALIZATIONR01HD020217 · NICHD · BOSTON UNIVERSITY MEDICAL CAMPUS · PI KAMINER, BENJAMIN · 1988 to 1990
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SYSTEMS AND INTEGRATIVE BIOLOGYT32GM007258 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GOLDBERG, ALFRED L · 1985 to 1994
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NICHD NIH HHS HD 20140NICHD NIH HHS HD 20217NIGMS NIH HHS T32 GMO7258-13
6 · The paper itself

Abstract

Using an antiserum produced against a purified calsequestrin-like (CSL) protein from a microsomal fraction of sea urchin eggs, we performed light and electron microscopic immunocytochemical localizations on sea urchin eggs and embryos in the first cell cycle. The sea urchin CSL protein has been found to bind Ca++ similarly to calsequestrin, the well-characterized Ca++ storage protein in the sarcoplasmic reticulum of muscle cells. In semi-thin frozen sections of unfertilized eggs, immunofluorescent staining revealed a tubuloreticular network throughout the cytoplasm. Staining of isolated egg cortices with the CSL protein antiserum showed the presence of a submembranous polygonal, tubular network similar to ER network patterns seen in other cells and in egg cortices treated with the membrane staining dye DiIC16[3]. In frozen sections of embryos during interphase of the first cell cycle, a cytoplasmic network similar to that of the unfertilized egg was present. During mitosis, we observed a dramatic concentration of the antibody staining within the asters of the mitotic apparatus where ER is known to aggregate. Electron microscopic localization on unfertilized eggs using peroxidase-labeled secondary antibody demonstrated the presence of the CSL protein within the luminal compartment of ER-like tubules. Finally, in frozen sections of centrifugally stratified eggs, the immunofluorescent staining concentrated in the clear zone: a layer highly enriched in ER and thought to be the site of calcium release upon fertilization. This localization of a CSL protein within the ER of the egg provides evidence for the ability of this organelle to serve a Ca++ storage role in the regulation of intracellular Ca++ in nonmuscle cells in general, and in the regulation of fertilization and cell division in sea urchin eggs in particular.

Indexed as

AnimalsBlotting, WesternCalcium-Binding ProteinsCalsequestrinCleavage Stage, OvumEndoplasmic ReticulumFluorescent Antibody TechniqueMitosisMolecular WeightMuscle ProteinsOvumSea UrchinsSpindle ApparatusCalcium-Binding ProteinsCalsequestrinMuscle Proteins

Identifiers

PMID2663877
PMCPMC2115469
OpenAlexW1996966664

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.