Unknown

Dataset Information

0

A role for the Cajal-body-associated SUMO isopeptidase USPL1 in snRNA transcription mediated by RNA polymerase II.


ABSTRACT: Cajal bodies are nuclear structures that are involved in biogenesis of snRNPs and snoRNPs, maintenance of telomeres and processing of histone mRNA. Recently, the SUMO isopeptidase USPL1 was identified as a component of Cajal bodies that is essential for cellular growth and Cajal body integrity. However, a cellular function for USPL1 is so far unknown. Here, we use RNAi-mediated knockdown in human cells in combination with biochemical and fluorescence microscopy approaches to investigate the function of USPL1 and its link to Cajal bodies. We demonstrate that levels of snRNAs transcribed by RNA polymerase (RNAP) II are reduced upon knockdown of USPL1 and that downstream processes such as snRNP assembly and pre-mRNA splicing are compromised. Importantly, we find that USPL1 associates directly with U snRNA loci and that it interacts and colocalises with components of the Little Elongation Complex, which is involved in RNAPII-mediated snRNA transcription. Thus, our data indicate that USPL1 plays a key role in RNAPII-mediated snRNA transcription.

SUBMITTER: Hutten S 

PROVIDER: S-EPMC3937775 | biostudies-literature | 2014 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

A role for the Cajal-body-associated SUMO isopeptidase USPL1 in snRNA transcription mediated by RNA polymerase II.

Hutten Saskia S   Chachami Georgia G   Winter Ulrike U   Melchior Frauke F   Lamond Angus I AI  

Journal of cell science 20140110 Pt 5


Cajal bodies are nuclear structures that are involved in biogenesis of snRNPs and snoRNPs, maintenance of telomeres and processing of histone mRNA. Recently, the SUMO isopeptidase USPL1 was identified as a component of Cajal bodies that is essential for cellular growth and Cajal body integrity. However, a cellular function for USPL1 is so far unknown. Here, we use RNAi-mediated knockdown in human cells in combination with biochemical and fluorescence microscopy approaches to investigate the func  ...[more]

Similar Datasets

| S-EPMC9758055 | biostudies-literature
| S-EPMC2196410 | biostudies-literature
2023-03-11 | PXD033638 | Pride
| S-EPMC1346915 | biostudies-literature
| S-EPMC4337070 | biostudies-literature
| S-EPMC4294624 | biostudies-literature
| S-EPMC8068570 | biostudies-literature
| S-EPMC6582409 | biostudies-literature
| S-EPMC3564262 | biostudies-literature
| S-EPMC2082468 | biostudies-literature