[The effect of extremely low frequency magnetic fields on cytochrome oxidase subunit 1 mRNA transcription].
← Research streamMF-1 cDNA sequence showed 100% homology with cytochrome oxidase subunit 1 (CO1). In HL-60, L1210 and CHL cells, exposure to 0.1 mT or 0.8 mT magnetic fields reduced CO1 transcription compared with controls after 20 minutes and after 24 hours (P<0.05).
Study snapshot
Abstract
OBJECTIVE: To clone and identify MF-1 gene which responded to extremely low frequency magnetic fields(ELF MF) in Daudi cells, and explore the response universality of MF-1 gene in several MF-sensitive cell lines, so as to provide experimental basis for revealing the mechanism of biological effects induced by magnetic field. METHODS: The DNA fragment of MF-1 was cloned and sequenced; the mRNA level of MF-1 gene were analysed in MF-sensitive cell lines(HL-60, L1210 and CHL) by Northern blot after these cells being treated with 0.1 mT and 0.8 mT MF for 20 minutes and 24 hours, respectively. RESULTS: The MF-1 cDNA sequence had 100% homology with cytochrome oxidase subunit 1 gene(CO1) by searching Gene Bank database; the transcription of CO1 in HL-60, L1210 and CHL cell lines which exposed to 0.1 mT and 0.8 mT MF for 20 minutes were significantly lower(0.38 +/- 0.12 and 0.37 +/- 0.04) than that of control(0.58 +/- 0.12) and so did for 24 hours exposure(0.46 +/- 0.09 and 0.45 +/- 0.09 vs 0.65 +/- 0.06) (P < 0.05). CONCLUSION: CO1 is a MF-responsive gene. Cytochrome oxidase activity may be affected through low level of CO1 transcription by magnetic fields, thus induce bioeffects in organisms.
AI evidence extraction
Structured fields below were generated from the paper’s abstract and metadata to make the evidence easier to inspect. Automated extraction may be incomplete or incorrect; verify important details against the original paper.
Main findings
MF-1 cDNA sequence showed 100% homology with cytochrome oxidase subunit 1 (CO1). In HL-60, L1210 and CHL cells, exposure to 0.1 mT or 0.8 mT magnetic fields reduced CO1 transcription compared with controls after 20 minutes and after 24 hours (P<0.05).
Outcomes measured
- MF-1 gene identification (homology to cytochrome oxidase subunit 1, CO1)
- CO1 mRNA transcription level (Northern blot)
Limitations
- In vitro study; relevance to human health outcomes not assessed
- Magnetic field frequency not reported in abstract
- Sample size/replicates not reported
- Only mRNA transcription measured; cytochrome oxidase activity inferred but not directly reported
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": null,
"sar_wkg": null,
"duration": "20 minutes and 24 hours"
},
"population": "Cell lines (Daudi; MF-sensitive cell lines HL-60, L1210, CHL)",
"sample_size": null,
"outcomes": [
"MF-1 gene identification (homology to cytochrome oxidase subunit 1, CO1)",
"CO1 mRNA transcription level (Northern blot)"
],
"main_findings": "MF-1 cDNA sequence showed 100% homology with cytochrome oxidase subunit 1 (CO1). In HL-60, L1210 and CHL cells, exposure to 0.1 mT or 0.8 mT magnetic fields reduced CO1 transcription compared with controls after 20 minutes and after 24 hours (P<0.05).",
"effect_direction": "harm",
"limitations": [
"In vitro study; relevance to human health outcomes not assessed",
"Magnetic field frequency not reported in abstract",
"Sample size/replicates not reported",
"Only mRNA transcription measured; cytochrome oxidase activity inferred but not directly reported"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"extremely low frequency",
"magnetic field",
"ELF MF",
"cytochrome oxidase subunit 1",
"CO1",
"mRNA transcription",
"Northern blot",
"Daudi cells",
"HL-60",
"L1210",
"CHL"
],
"suggested_hubs": [
{
"slug": "occupational-exposure",
"weight": 0.55,
"reason": "Published in an industrial hygiene/occupational diseases journal and studies ELF magnetic field bioeffects relevant to occupational contexts."
}
]
}AI-extracted fields are generated from the abstract and metadata and may be incomplete or incorrect. This material is for informational purposes and is not medical advice.
Identifiers and source
DOI: Not supplied
PubMed: 14694645
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