Description: A DNA sequence encoding the human C1D (Q13901) (Met 1-Ser 141) was fused with the GST tag at the N-terminus.
NCBI and Uniprot Product Information
NCBI Description
The protein encoded by this gene is a DNA binding and apoptosis-inducing protein and is localized in the nucleus. It is also a Rac3-interacting protein which acts as a corepressor for the thyroid hormone receptor. This protein is thought to regulate TRAX/Translin complex formation. Alternate splicing results in multiple transcript variants that encode the same protein. Multiple pseudogenes of this gene are found on chromosome 10.[provided by RefSeq, Jun 2010]
Uniprot Description
C1D: Plays a role in the recruitment of the RNA exosome complex to pre-rRNA to mediate the 3'-5' end processing of the 5.8S rRNA; this function may include MPHOSPH6. Can activate PRKDC not only in the presence of linear DNA but also in the presence of supercoiled DNA. Can induce apoptosis in a p53/TP53 dependent manner. May regulate the TRAX/TSN complex formation. Potentiates transcriptional repression by NR1D1 and THRB. Belongs to the C1D family.
Protein type: DNA-binding; Nuclear receptor co-regulator; Nucleolus; Transcription, coactivator/corepressor
Chromosomal Location of Human Ortholog: 2p14
Cellular Component: nuclear exosome (RNase complex); nucleolus; nucleoplasm; nucleus
Molecular Function: protein binding; RNA binding
Biological Process: maturation of 5.8S rRNA; rRNA processing