<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR626/009/SRR6262169/SRR6262169_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR626/000/SRR6262170/SRR6262170_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR626/008/SRR6262168/SRR6262168_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR626/001/SRR6262171/SRR6262171_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR626/008/SRR6262168/SRR6262168_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR626/001/SRR6262171/SRR6262171_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR626/000/SRR6262170/SRR6262170_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR626/009/SRR6262169/SRR6262169_1.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>The Ohio State University</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA416813</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Fhit is a tumor suppressor/genomic protective protein that is lost in more than 50% of cancers but the mechanism by which it works is unknown. Unlike most tumor suppressors Fhit is a cytoplasmic protein with no known interacting partners. A previous study found that Fhit regulates the translation of thymidine kinase 1 (TK1) mRNA into protein, with greater TK1 translation in Fhit-positive versus Fhit-negative cells. Increased TK1 translation was dependent on the ability of Fhit to degrade small RNA fragments termed nucleoside 5’,5’-triphosphates. The goal of this study was to identify mRNAs whose translation is regulated by Fhit, and use this information to identify the proteins that are responsible for its tumor suppressor/genome protective effects.</long_description><repository>ENA</repository><name_synonyms>Human, strain, H1299, human being, Man (Taxonomy), Homo sapiens, CRL-5803., Modern Man, Modern, cultivar, NCI-H1299, man, Man, ecotype, human</name_synonyms><description_synonyms>preventive measures, Fra14A2, Controlling, FRA3B, preventive therapy, Polyribosome, AW045638, reference sample, control, determination, prophylaxis, AP3Aase, polyribosome, chemical analysis., assay, prevention and control, Polysomes, Polysome, Controlled, prevention</description_synonyms></additional><is_claimable>false</is_claimable><name>Homo sapiens cultivar:NCI-H1299</name><description>Identification of mRNAs under translational control by Fhit using polysome gradient analysis</description><dates><last_updated>2025-09-24</last_updated><first_public>2017-11-10</first_public></dates><accession>PRJNA416813</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>