NIPBL

Nipped-B-like protein (NIPBL), also known as SCC2 or delangin is a protein that in humans is encoded by the NIPBL gene.[5] NIPBL is required for the association of cohesin with DNA and is the major subunit of the cohesin loading complex.[6] Heterozygous mutations in NIPBL account for an estimated 60% of case of Cornelia de Lange Syndrome.[7]

NIPBL
Identifiers
Aliases	NIPBL, CDLS, CDLS1, IDN3, IDN3-B, Scc2, cohesin loading factor, NIPBL cohesin loading factor
External IDs	OMIM: 608667 MGI: 1913976 HomoloGene: 15850 GeneCards: NIPBL
Gene location (Human) Chr. Chromosome 5 (human)[1] Band 5p13.2 Start 36,876,769 bp[1] End 37,066,413 bp[1]
Gene location (Mouse) Chr. Chromosome 15 (mouse)[2] Band 15|15 A1 Start 8,290,617 bp[2] End 8,444,463 bp[2]
Gene ontology Molecular function • mediator complex binding • chromo shadow domain binding • protein N-terminus binding • histone deacetylase binding • chromatin binding • protein C-terminus binding • GO:0001948 protein binding Cellular component • SMC loading complex • nucleoplasm • chromatin • extracellular exosome • cell nucleus • integrator complex • nuclear chromosome • nuclear chromatin • chromosome • Scc2-Scc4 cohesin loading complex Biological process • positive regulation of histone deacetylation • forelimb morphogenesis • eye morphogenesis • regulation of embryonic development • cognition • uterus morphogenesis • cellular response to X-ray • regulation of developmental growth • heart morphogenesis • outflow tract morphogenesis • positive regulation of ossification • negative regulation of transcription from RNA polymerase II promoter • sensory perception of sound • cellular response to DNA damage stimulus • stem cell population maintenance • ear morphogenesis • cellular protein localization • heart development • brain development • developmental growth • external genitalia morphogenesis • regulation of hair cycle • positive regulation of multicellular organism growth • embryonic digestive tract morphogenesis • gall bladder development • regulation of gene expression • embryonic cranial skeleton morphogenesis • embryonic viscerocranium morphogenesis • cell cycle • metanephros development • negative regulation of transcription, DNA-templated • fat cell differentiation • maintenance of mitotic sister chromatid cohesion • embryonic forelimb morphogenesis • face morphogenesis • positive regulation of transcription from RNA polymerase II promoter • regulation of transcription from RNA polymerase II promoter • positive regulation of neuron migration • transcription, DNA-templated • regulation of transcription, DNA-templated • multicellular organism development • mitotic sister chromatid cohesion • double-strand break repair • mitotic chromosome condensation • establishment of mitotic sister chromatid cohesion • rDNA condensation • establishment of protein localization to chromatin • transcriptional activation by promoter-enhancer looping • cohesin loading • positive regulation of mitotic cohesin loading • replication-born double-strand break repair via sister chromatid exchange Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	25836	71175
Ensembl	ENSG00000164190	ENSMUSG00000022141
UniProt	Q6KC79	Q6KCD5
RefSeq (mRNA)	NM_015384 NM_133433	NM_027707 NM_201232
RefSeq (protein)	NP_056199 NP_597677	NP_081983 NP_957684
Location (UCSC)	Chr 5: 36.88 – 37.07 Mb	Chr 15: 8.29 – 8.44 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Structure and Interactions

Structure of SCC4 (green) in complex with SCC2 N-terminal domain (blue) from budding yeast (Hinshaw et al., 2015)

NIPBL is a large hook-shaped protein containing HEAT repeats.[8] NIPBL forms a complex with MAU2 (Scc4 in budding yeast) known as the cohesin loading complex.[9] As this name suggests NIPBL and MAU2 are required for the initial association of cohesin with DNA.

Cohesin is thought to mediate enhancer-promoter interactions and generate Topologically associating domain. As well as mediating cohesion and regulating DNA architecture the cohesin complex is required for DNA repair by homologous recombination. Given that NIPBL is required for cohesin's association with DNA it is thought that NIPBL is also required for all of these processes. Consistently, inactivation of Nipbl results in the loss topologically associating domains[10] and cohesion.[11]

NIPBL binds dynamically to chromatin principally through an association with cohesin.[12] NIPBL’s movement within chromatin is consistent with a mechanism involving hopping between chromosomal cohesin rings. A cohesin-independent function in the regulation of gene expression has also been demonstrated for NIPBL.[13][14]

Clinical significance

Mutations in this gene result in Cornelia de Lange syndrome (CdLS), a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and mental retardation.[5] As these mutations are usually heterozygous, CdLS is caused by a reduction in the abundance of Nipbl not a complete loss. Experiments on cells from patients and mice indicate that the reduction is by less than half.[15] It is not known why a reduction in Nipbl expression results in CdLS.

References

1. GRCh38: Ensembl release 89: ENSG00000164190 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000022141 - Ensembl, May 2017
3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
5. "Entrez Gene: Nipped-B homolog (Drosophila)".
6. Ciosk R, Shirayama M, Shevchenko A, Tanaka T, Toth A, Shevchenko A, Nasmyth K (2000). "Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins". Molecular Cell. 5 (2): 243–54. doi:10.1016/S1097-2765(00)80420-7. PMID 10882066.
7. Rohatgi S, Clark D, Kline AD, Jackson LG, Pie J, Siu V, Ramos FJ, Krantz ID, Deardorff MA (July 2010). "Facial diagnosis of mild and variant CdLS: Insights from a dysmorphologist survey". American Journal of Medical Genetics. Part A. 152A (7): 1641–53. doi:10.1002/ajmg.a.33441. PMC 4133091. PMID 20583156.
8. Kikuchi S, Borek DM, Otwinowski Z, Tomchick DR, Yu H (November 2016). "Crystal structure of the cohesin loader Scc2 and insight into cohesinopathy". Proceedings of the National Academy of Sciences of the United States of America. 113 (44): 12444–12449. doi:10.1073/pnas.1611333113. PMC 5098657. PMID 27791135.
9. Nasmyth K (October 2011). "Cohesin: a catenase with separate entry and exit gates?". Nature Cell Biology. 13 (10): 1170–7. doi:10.1038/ncb2349. PMID 21968990. S2CID 25382204.
10. Schwarzer W, Abdennur N, Goloborodko A, Pekowska A, Fudenberg G, Loe-Mie Y, Fonseca NA, Huber W, Haering C, Mirny L, Spitz F (15 December 2016). "Two independent modes of chromosome organization are revealed by cohesin removal". p. 094185. bioRxiv 10.1101/094185.
11. Ciosk R, Shirayama M, Shevchenko A, Tanaka T, Toth A, Shevchenko A, Nasmyth K (February 2000). "Cohesin's binding to chromosomes depends on a separate complex consisting of Scc2 and Scc4 proteins". Molecular Cell. 5 (2): 243–54. doi:10.1016/s1097-2765(00)80420-7. PMID 10882066.
12. Rhodes J, Mazza D, Nasmyth K, Uphoff S (2017). "Scc2/Nipbl hops between chromosomal cohesin rings after loading". eLife. 6. doi:10.7554/eLife.30000. PMC 5621834. PMID 28914604.
13. Zuin J, Franke V, van Ijcken WF, van der Sloot A, Krantz ID, van der Reijden MI, Nakato R, Lenhard B, Wendt KS (February 2014). "A cohesin-independent role for NIPBL at promoters provides insights in CdLS". PLOS Genetics. 10 (2): e1004153. doi:10.1371/journal.pgen.1004153. PMC 3923681. PMID 24550742.
14. van den Berg DL, Azzarelli R, Oishi K, Martynoga B, Urbán N, Dekkers DH, Demmers JA, Guillemot F (January 2017). "Nipbl Interacts with Zfp609 and the Integrator Complex to Regulate Cortical Neuron Migration". Neuron. 93 (2): 348–361. doi:10.1016/j.neuron.2016.11.047. PMC 5263256. PMID 28041881.
15. Kawauchi S, Calof AL, Santos R, Lopez-Burks ME, Young CM, Hoang MP, Chua A, Lao T, Lechner MS, Daniel JA, Nussenzweig A, Kitzes L, Yokomori K, Hallgrimsson B, Lander AD (September 2009). "Multiple organ system defects and transcriptional dysregulation in the Nipbl(+/-) mouse, a model of Cornelia de Lange Syndrome". PLOS Genetics. 5 (9): e1000650. doi:10.1371/journal.pgen.1000650. PMC 2730539. PMID 19763162.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.