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
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.