The human ELL gene on chromosome 19 undergoes frequent translocations
with the trithorax-like MLL gene on chromosome 11 in acute myeloid leu
kemias. Here, ELL was shown to encode a previously uncharacterized elo
ngation factor that can increase the catalytic rate of RNA polymerase
II transcription by suppressing transient pausing by polymerase at mul
tiple sites along the DNA. Functionally, ELL resembles Elongin (SIII),
a transcription elongation factor regulated by the product of the von
Hippel-Lindau (VHL) tumor suppressor gene. The discovery of a second
elongation factor implicated in oncogenesis provides further support f
or a close connection between the regulation of transcription elongati
on and cell growth.