developmental stage:Expressed during embryogenesis. ,Disease:May play a part in the etiology of the DiGeorge syndrome (DGS) , a developmental disorder due to an abnormal development of the third and fourth pharyngeal pouches. The clinical features include absence or hypoplasia of the thymus and parathyroid glands , cardiovascular malformations , facial dysplasia , a cleft palate and mental retardation. ,Function:Cooperates with ASF1A to promote replication-independent chromatin assembly. Required for the periodic repression of histone gene transcription during the cell cycle. Required for the formation of senescence-associated heterochromatin foci (SAHF) and efficient senescence-associated cell cycle exit. ,PTM:Phosphorylated by CDK2/CCNA1 and CDK2/CCNE1 on Thr-555 in vitro. Also phosphorylated on Thr-555 and Ser-687 in vivo. ,PTM:Sumoylated. ,similarity:Belongs to the WD repeat HIR1 family. ,similarity:Contains 8 WD repeats. ,subcellular location:Primarily , though not exclusively , localized to the nucleus. Localizes to PML bodies immediately prior to onset of senescence. ,subunit:Interacts with histone H3F3B , PAX3 and PAX7 (By similarity) . Interacts with CCNA1 , HIRIP3 , NFU1/HIRIP5 and histone H2B. Part of a complex which includes ASF1A , CABIN1 , histone H3.3 , histone H4 and UBN1. ,tissue specificity:Expressed at high levels in kidney , pancreas and skeletal muscle and at lower levels in brain , heart , liver , lung , and placenta. ,
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