======= CDYL ======= == Gene Information == * **Official Symbol**: CDYL * **Official Name**: chromodomain Y like * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=9425|9425]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9Y232|Q9Y232]] * **Interactions**: [[https://thebiogrid.org/search.php?search=CDYL&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20CDYL|Open PubMed]] * **OMIM**: [[https://omim.org/entry/603778|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Isoform 2: Chromatin reader protein that recognizes and binds histone H3 trimethylated at 'Lys-9', dimethylated at 'Lys- 27' and trimethylated at 'Lys-27' (H3K9me3, H3K27me2 and H3K27me3, respectively) (PubMed:19808672, PubMed:28402439). Part of multimeric repressive chromatin complexes, where it is required for transmission and restoration of repressive histone marks, thereby preserving the epigenetic landscape (PubMed:28402439). Required for chromatin targeting and maximal enzymatic activity of Polycomb repressive complex 2 (PRC2); acts as a positive regulator of PRC2 activity by bridging the pre-existing histone H3K27me3 and newly recruited PRC2 on neighboring nucleosomes (PubMed:22009739). Acts as a corepressor for REST by facilitating histone-lysine N- methyltransferase EHMT2 recruitment and H3K9 dimethylation at REST target genes for repression (PubMed:19061646). Involved X chromosome inactivation in females: recruited to Xist RNA-coated X chromosome and facilitates propagation of H3K9me2 by anchoring EHMT2 (By similarity). Required for neuronal migration during brain development by repressing expression of RHOA (By similarity). In addition to act as a chromatin reader, acts as a hydro-lyase (PubMed:28803779). Shows crotonyl-coA hydratase activity by mediating the conversion of crotonyl-CoA ((2E)- butenoyl-CoA) to beta-hydroxybutyryl-CoA (3-hydroxybutanoyl-CoA), thereby acting as a negative regulator of histone crotonylation (PubMed:28803779). Histone crotonylation is required during spermatogenesis; down-regulation of histone crotonylation by CDYL regulates the reactivation of sex chromosome-linked genes in round spermatids and histone replacement in elongating spermatids (By similarity). {ECO:0000250|UniProtKB:Q9WTK2, ECO:0000269|PubMed:19061646, ECO:0000269|PubMed:19808672, ECO:0000269|PubMed:22009739, ECO:0000269|PubMed:28402439, ECO:0000269|PubMed:28803779}. Isoform 3: Not able to recognize and bind histone H3K9me3, histone H3K27me2 and histone H3K27me3, due to the absence of the chromo domain (PubMed:19808672). Acts as a negative regulator of isoform 2 by displacing isoform 2 from chromatin. {ECO:0000269|PubMed:19808672}. |ECH| |Chromo| |negative regulation of peptidyl-lysine crotonylation| |regulation of peptidyl-lysine crotonylation| |crotonyl-CoA hydratase activity| |random inactivation of X chromosome| |dosage compensation by inactivation of X chromosome| |dosage compensation| |methylated histone binding| |protein binding, bridging| |chromosome| |spermatid development| |spermatid differentiation| |regulation of gene expression, epigenetic| |transcription corepressor activity| |germ cell development| |cellular process involved in reproduction in multicellular organism| |chromatin binding| |nuclear speck| |spermatogenesis| |male gamete generation| |negative regulation of protein modification process| |developmental process involved in reproduction| |gamete generation| |multicellular organismal reproductive process| |sexual reproduction| |multicellular organism reproduction| |multi-organism reproductive process| |negative regulation of cellular protein metabolic process| |negative regulation of protein metabolic process| |negative regulation of nucleic acid-templated transcription| |negative regulation of RNA biosynthetic process| |negative regulation of RNA metabolic process| |reproductive process| |reproduction| |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| |cell development| |regulation of protein modification process| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp47|Lapatinib 5μM R01 exp47]]|-1.78| |[[:results:exp40|2-Methoxyestradiol 0.2μM R01 exp40]]|-1.77| |[[:results:exp470|Chloroquine 32μM R08 exp470]]|1.76| |[[:results:exp488|Hippuristanol 0.12μM R08 exp488]]|1.78| |[[:results:exp184|Ixabepilone 0.004 to 0.005μM on day4 R04 exp184]]|1.88| |[[:results:exp444|THZ531 0.225μM R08 exp444]]|1.92| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 0/726 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/25| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/15| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/14| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/7| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 4529 * **Expression level (log2 read counts)**: 5.93 {{:chemogenomics:nalm6 dist.png?nolink |}}