Evidence map›Paper›PMID 8616221›Full record

ArticlePlant molecular biology1995

Increased transcript levels of a methionine synthase during adhesion-induced activation of Chlamydomonas reinhardtii gametes.

V Kurvari, F Qian, W J Snell

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Plant molecular biology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.5field-weighted citation impact, top 36% 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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Proteomic analysis of a eukaryotic cilium.The Journal of cell biology · 2005
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Analysis of xylem formation in pine by cDNA sequencing.Proceedings of the National Academy of Sciences of the United States of America · 1998
    Article
  14. The specific features of methionine biosynthesis and metabolism in plants.Proceedings of the National Academy of Sciences of the United States of America · 1998
    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

3 authors at 1 institution in 1 country.

V KurvariDepartment of Cell Biology and Neuroscience, University of Texas Southwestern Medical Center, Dallas 75235-9039, USA.
F Qian
W J Snell
The University of Texas Southwestern Medical Center · US

Funding

CELL SURFACE RECOGNITION AND CELL INTERACTIONSR01GM025661 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI SNELL, WILLIAM J · 1985 to 2017
$5.9M
MAPPING OF IG MUTATIONS BY HOMOLOGOUS RECOMBINATIONR01GM035341 · NIGMS · UNIVERSITY OF TORONTO · PI SHULMAN, MARC J · 1985 to 1990
–
NIGMS NIH HHS GM35341NIGMS NIH HHS R01 GM025661
6 · The paper itself

Abstract

Chlamydomonas gametes of opposite mating types interact through flagellar adhesion molecules called agglutinins leading to a signal transduction cascade that induces cell wall loss and activation of mating structures along with other cellular responses that ultimately result in zygote formation. To identify molecules involved in these complex cellular events, we have employed subtractive and differential hybridization with cDNA from mt+ gametes activated for fertilization and non-signaling, vegetative (non-gametic) cells. We identified 55 cDNA clones whose transcripts were regulated in activated gametes. Here we report the molecular cloning and characterization of the complementary DNA (cDNA) for one clone whose transcripts in activated gametes were several-fold higher than in normal gametes. Regulation of the transcript was not related simply to protein synthesis because it was not increased in cells synthesizing new cell wall proteins. The cDNA contained a single open reading frame (ORF) of 815 amino acids encoding a polypeptide of calculated relative mass of 87 kDa. Database search analysis and sequence alignment indicated that the deduced amino acid sequence exhibited 42% identity and 62% similarity to a class of prokaryotic methyl transferases (5-methyltetrahydrofolate-homocysteine methyl transferase; EC 2.1.1.14) known to be involved in the terminal step of de novo biosynthesis of methionine. This enzyme catalyzes transfer of a methyl group from 5-methyltetrahydrofolate to homocysteine resulting in methionine formation. Affinity-purified polyclonal antibodies raised against a bacterially produced GST-fusion protein identified a 85 kDa soluble protein in Chlamydomonas gametes. Southern blot hybridization indicated that the enzyme is encoded by a single-copy gene. The evidence presented in this paper raises the possibility that, in addition to its participation in de novo biosynthesis and regeneration of methionine, Chlamydomonas methionine synthase may play a role in adhesion-induced events during fertilization.

Indexed as

Gene Expression Regulation, PlantTranscription, Genetic5-Methyltetrahydrofolate-Homocysteine S-MethyltransferaseAmino Acid SequenceAnimalsBase SequenceCell AdhesionChlamydomonas reinhardtiiCloning, MolecularConserved SequenceDNA, ComplementaryDNA PrimersEscherichia coliFertilizationGene Expression Regulation, EnzymologicGene Library5-Methyltetrahydrofolate-Homocysteine S-MethyltransferaseDNA, ComplementaryDNA PrimersGlutathione TransferaseRecombinant Fusion Proteins

Identifiers

PMID8616221
OpenAlexW2050900835

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.