======= OBFC1 ======= == Gene Information == * **Official Symbol**: STN1 * **Official Name**: STN1 subunit of CST complex * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=79991|79991]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9H668|Q9H668]] * **Interactions**: [[https://thebiogrid.org/search.php?search=OBFC1&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20OBFC1|Open PubMed]] * **OMIM**: [[https://omim.org/entry/613128|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Component of the CST complex proposed to act as a specialized replication factor promoting DNA replication under conditions of replication stress or natural replication barriers such as the telomere duplex. The CST complex binds single-stranded DNA with high affinity in a sequence-independent manner, while isolated subunits bind DNA with low affinity by themselves. Initially the CST complex has been proposed to protect telomeres from DNA degradation (PubMed:19854130). However, the CST complex has been shown to be involved in several aspects of telomere replication. The CST complex inhibits telomerase and is involved in telomere length homeostasis; it is proposed to bind to newly telomerase-synthesized 3' overhangs and to terminate telomerase action implicating the association with the ACD:POT1 complex thus interfering with its telomerase stimulation activity. The CST complex is also proposed to be involved in fill-in synthesis of the telomeric C-strand probably implicating recruitment and activation of DNA polymerase alpha (PubMed:22964711, PubMed:22763445). The CST complex facilitates recovery from many forms of exogenous DNA damage; seems to be involved in the re- initiation of DNA replication at repaired forks and/or dormant origins (PubMed:25483097). Required for efficicient replication of the duplex region of the telomere. Promotes efficient replication of lagging-strand telomeres (PubMed:22863775, PubMed:22964711). Promotes general replication start following replication-fork stalling implicating new origin firing (PubMed:22863775). May be in involved in C-strand fill-in during late S/G2 phase independent of its role in telomere duplex replication (PubMed:23142664). {ECO:0000269|PubMed:19648609, ECO:0000269|PubMed:19854130, ECO:0000269|PubMed:22763445, ECO:0000269|PubMed:22863775, ECO:0000269|PubMed:22964711, ECO:0000269|PubMed:23142664, ECO:0000269|PubMed:25483097, ECO:0000305|PubMed:23851344}. |DUF1879| |tRNA anti| |CST complex| |single-stranded telomeric DNA binding| |telomere capping| |negative regulation of telomere maintenance via telomerase| |negative regulation of telomere maintenance via telomere lengthening| |telomeric DNA binding| |telomere maintenance via telomere lengthening| |positive regulation of DNA replication| |negative regulation of telomere maintenance| |negative regulation of DNA biosynthetic process| |intermediate filament cytoskeleton| |regulation of telomere maintenance via telomerase| |regulation of telomere maintenance via telomere lengthening| |regulation of telomere maintenance| |telomere maintenance| |telomere organization| |single-stranded DNA binding| |regulation of DNA replication| |nuclear chromosome, telomeric region| |regulation of DNA biosynthetic process| |negative regulation of DNA metabolic process| |fibrillar center| |negative regulation of chromosome organization| |anatomical structure homeostasis| |regulation of chromosome organization| |regulation of DNA metabolic process| |negative regulation of organelle organization| |intracellular membrane-bounded organelle| |negative regulation of cellular component organization| |DNA metabolic process| |chromosome organization| |regulation of organelle organization| |negative regulation of cellular macromolecule biosynthetic process| |negative regulation of nucleobase-containing compound metabolic process| |negative regulation of macromolecule biosynthetic process| |negative regulation of cellular biosynthetic process| |negative regulation of biosynthetic process| |homeostatic process| |positive regulation of macromolecule biosynthetic process| |positive regulation of cellular biosynthetic process| |positive regulation of biosynthetic process| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp360|Genistein 15μM R07 exp360]]|-1.93| |[[:results:exp27|Pimelic-diphenylamide-106 0.5μM R00 exp27]]|-1.91| |[[:results:exp1|5-Fluorouracil 2μM R00 exp1]]|-1.83| ^Gene^Correlation^ |[[:human genes:t:ten1|TEN1]]|0.539| |[[:human genes:c:ctc1|CTC1]]|0.477| |[[:human genes:t:thg1l|THG1L]]|0.428| |[[:human genes:e:eif3f|EIF3F]]|0.427| |[[:human genes:g:gmppb|GMPPB]]|0.407| |[[:human genes:u:uap1|UAP1]]|0.403| |[[:human genes:t:trmt61a|TRMT61A]]|0.402| Global Fraction of Cell Lines Where Essential: 45/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|1/28| |blood|4/28| |bone|2/26| |breast|4/33| |central nervous system|5/56| |cervix|0/4| |colorectal|2/17| |esophagus|1/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|1/20| |lung|5/75| |lymphocyte|1/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|1/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|4/22| |urinary tract|2/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 1557 * **Expression level (log2 read counts)**: 3.34 {{:chemogenomics:nalm6 dist.png?nolink |}}