Evidence map›Paper›PMID 36911915›Full record

ArticleG3 (Bethesda, Md.)2023

A molecular cell biology toolkit for the study of meiosis in the silkworm Bombyx mori.

Youbin Xiang, Dai Tsuchiya, Fengli Guo, Jennifer Gardner, Scott McCroskey, Andrew Price, Eelco C Tromer, James R Walters, Cathleen M Lake, R Scott Hawley

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Programmed meiotic errors facilitate dichotomous sperm production in the silkworm,Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
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

10 authors at 3 institutions in 2 countries.

Youbin XiangStowers Institute for Medical Research, Kansas City, MO 64110, USA.ORCID 0009-0005-1166-080X
Dai TsuchiyaStowers Institute for Medical Research, Kansas City, MO 64110, USA.ORCID 0000-0001-8385-2775
Fengli GuoStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Jennifer GardnerStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Scott McCroskeyStowers Institute for Medical Research, Kansas City, MO 64110, USA.
Andrew PriceStowers Institute for Medical Research, Kansas City, MO 64110, USA.ORCID 0000-0001-9080-1802
Eelco C TromerFaculty of Science and Engineering, Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Groningen 9747 AG, The Netherlands.ORCID 0000-0003-3540-7727
James R WaltersDepartment of Ecology and Evolutionary Biology, University of Kansas, Lawrence, KS 66045, USA.ORCID 0000-0002-6340-995X
Cathleen M LakeStowers Institute for Medical Research, Kansas City, MO 64110, USA.ORCID 0000-0002-8196-8464
R Scott HawleyStowers Institute for Medical Research, Kansas City, MO 64110, USA.ORCID 0000-0002-6478-0494
Stowers Institute for Medical Research · USUniversity of Groningen · NLUniversity of Kansas · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meiosis is usually described as 4 essential and sequential processes: (1) homolog pairing; (2) synapsis, mediated by the synaptonemal complex; (3) crossing over; and (4) segregation. In this canonical model, the maturation of crossovers into chiasmata plays a vital role in holding homologs together and ensuring their segregation at the first meiotic division. However, Lepidoptera (moths and butterflies) undergo 3 distinct meiotic processes, only one of which is canonical. Lepidoptera males utilize 2 meiotic processes: canonical meiosis that produces nucleated fertile sperm, and a noncanonical meiosis that produces anucleated nonfertile sperm which are nonetheless essential for reproduction. Lepidoptera females, which carry heteromorphic sex chromosomes, undergo a completely achiasmate (lacking crossovers) meiosis, thereby requiring an alternative mechanism to ensure proper homolog segregation. Here, we report that the development of a molecular cell biology toolkit designed to properly analyze features of meiosis, including the synaptonemal complex structure and function, in the silkworm Bombyx mori. In addition to standard homology searches to identify Bombyx orthologs of known synaptonemal complex encoding genes, we developed an ortholog discovery app (Shinyapp) to identify Bombyx orthologs of proteins involved in several meiotic processes. We used this information to clone genes expressed in the testes and then created antibodies against their protein products. We used the antibodies to confirm the localization of these proteins in normal male spermatocytes, as well as using in vitro assays to confirm orthologous interactions. The development of this toolkit will facilitate further study of the unique meiotic processes that characterize meiosis in Lepidoptera.

Indexed as

BombyxButterfliesAnimalsChromosome PairingFemaleMaleMeiosisSemenSex ChromosomesSynaptonemal ComplexBombyx moriHOP1LepidopterameiosisPCH2SYCP1SYCP2SYCP3synaptonemal complex

Identifiers

PMID36911915
PMCPMC10151401
OpenAlexW4324021060

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.