Identification, cloning, expression, and biochemical characterization of the testis-specific RNA polymerase II elongation factor ELL3

Citation
T. Miller et al., Identification, cloning, expression, and biochemical characterization of the testis-specific RNA polymerase II elongation factor ELL3, J BIOL CHEM, 275(41), 2000, pp. 32052-32056
Citations number
33
Categorie Soggetti
Biochemistry & Biophysics
Journal title
JOURNAL OF BIOLOGICAL CHEMISTRY
ISSN journal
00219258 → ACNP
Volume
275
Issue
41
Year of publication
2000
Pages
32052 - 32056
Database
ISI
SICI code
0021-9258(20001013)275:41<32052:ICEABC>2.0.ZU;2-3
Abstract
The human ELL gene, which is a frequent target for translocation in acute m yeloid leukemia, was initially isolated from rat liver nuclei and found to be an RNA polymerase II elongation factor. Based on homology to ELL, we lat er cloned ELL2 and demonstrated that it can also increase the catalytic rat e of transcription elongation by RNA polymerase II. To better understand th e role of ELL proteins in the regulation of transcription by RNA polymerase II, we have initiated a search for proteins related to ELLs. In this repor t, we describe the molecular cloning, expression, and characterization of E LL3, a novel RNA polymerase II elongation factor approximately 50% similar to both ELL and ELL2. Our transcriptional studies have demonstrated that EL LS can also increase the catalytic rate of transcription elongation by RNA polymerase II, The C-terminal domain of ELL, which we recently demonstrated to be required and sufficient for the immortalization of myeloid progenito r cells, shares strong similarities to the C-terminal domain of ELL3. ELL3 was localized by immunofluorescence to the nucleus of cells, and Northern a nalysis indicated that ELL3 is a testis-specific RNA polymerase II elongati on factor.