Evidence map›Paper›PMID 36892215›Full record

ArticleBiochemical Society transactions2023

Regulation of germline proteostasis by HSF1 and insulin/IGF-1 signaling.

Tahir Muhammad, Jian Li

Open access · greenAbstract read
In one paragraph

Article in Biochemical Society transactions, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

1 citing paper in PubMed, 6 citations in OpenAlex.

  1. 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

2 authors at 1 institution in 1 country.

Tahir MuhammadDepartment of Cell Biology and Anatomy, New York Medical College, 15 Dana Road, Valhalla, NY, U.S.A.
Jian LiDepartment of Cell Biology and Anatomy, New York Medical College, 15 Dana Road, Valhalla, NY, U.S.A.ORCID 0000-0001-5168-6610
New York Medical College · US

Funding

Roles of heat shock transcriptional factor 1 in cell proliferation independent of the heat shock responseR35GM138364 · NIGMS · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI LI, JIAN · 2020 to 2024
$2.1M
NIGMS NIH HHS R35 GM138364
6 · The paper itself

Abstract

Protein homeostasis (proteostasis) is essential for cellular function and organismal health and requires the concerted actions of protein synthesis, folding, transport, and turnover. In sexually reproducing organisms, the immortal germline lineage passes genetic information across generations. Accumulating evidence indicates the importance of proteome integrity for germ cells as genome stability. As gametogenesis involves very active protein synthesis and is highly energy-demanding, it has unique requirements for proteostasis regulation and is sensitive to stress and nutrient availability. The heat shock factor 1 (HSF1), a key transcriptional regulator of cellular response to cytosolic and nuclear protein misfolding has evolutionarily conserved roles in germline development. Similarly, insulin/insulin-like growth factor-1 (IGF-1) signaling, a major nutrient-sensing pathway, impacts many aspects of gametogenesis. Here, we focus on HSF1 and IIS to review insights into their roles in germline proteostasis and discuss the implications on gamete quality control during stress and aging.

Indexed as

Germ CellsInsulin-Like Growth Factor IInsulinsProteostasisSignal TransductionInsulin-Like Growth Factor IInsulinsgametogenesisHSF1insulin/IGF-1 signalingproteostasisstress response

Identifiers

PMID36892215
PMCPMC10355142
OpenAlexW4323653253

What OpenQuestion holds

Textmetadata
LicenceTDM
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.