Nipped-B-like protein (NIPBL), also known as SCC2 or delangin is a
protein that in humans is encoded by the NIPBLgene.[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]
Structure and Interactions
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 domains (TADs). 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.
^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.
bioRxiv10.1101/094185.