{"database":"ENA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Fastqsanger.gz":["ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR224/054/SRR22483854/SRR22483854_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR224/053/SRR22483853/SRR22483853_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR224/051/SRR22483851/SRR22483851_2.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR224/052/SRR22483852/SRR22483852_2.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR224/051/SRR22483851/SRR22483851_1.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR224/054/SRR22483854/SRR22483854_2.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR224/053/SRR22483853/SRR22483853_2.fastq.gz","ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR224/052/SRR22483852/SRR22483852_1.fastq.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["Nanjing First Hospital"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA907308"],"scientific_name":["Homo sapiens"],"long_description":["5-fluorouracil (5‑FU) based chemotherapy is the first-line chemotherapy scheme for CRC, whereas acquired drug resistance poses a huge obstacle to curing CRC patients and the mechanism is still obscure. METTL14 is a core subunit of the m6A methyltransferase complex and has been reported to regulate the drug resistance of cancers. Here, we demonstrated that METTL14 is significantly downregulated in 5-FU-resistant CRC and METTL14 overexpression inhibits the proliferation and 5-FU resistance of CRC cells in vitro and in vivo. In addition, we found that MIB1 catalyzes the K63-linked ubiquitination of METTL14 and induces its degradation through the autolysosome pathway, while AURKA-mediated phosphorylation enhances METTL14 stability by inhibiting its ubiquitination. Moreover, we first discovered that METTL14 functions in 5-FU-resistant CRC cells by directly participating in the translation initiation of non-m6A-modified mRNAs independently of METTL3, rather than cooperating with METTL3 to methylate adenosine residues of targets. Further analysis indicated that METTL14 regulates the cell cycle process in 5-FU-resistant CRC cells. Collectively, our study not only identified METTL14 as a potential therapeutic target for 5-FU resistance in CRC but also revealed a novel translation-facilitating role of METTL14. Overall design: METTL14 overexpression plasmids and negative control plasmids were transfected into 5-FU-resistant HCT-8 cells, respectively. Then cells were treated with 100ug/mL CHX and implemented to the transcription sequencing. Experiments were performed twice independently."],"repository":["ENA"],"additional_accession":[]},"is_claimable":false,"name":"The post-translational modifications and translation-regulatory role of METTL14 in 5-fluorouracil-resistant colorectal cancer [mRNA-seq]","description":"The post-translational modifications and translation-regulatory role of METTL14 in 5-fluorouracil-resistant colorectal cancer [mRNA-seq]","dates":{"last_updated":"2025-09-24","first_public":"2023-12-02"},"accession":"PRJNA907308","cross_references":{"GEO":["GSE219171"],"taxon":["9606"]}}