Abstract
Rpb11 subunit of RNA polymerase II of Eukaryotes is related to N-terminal domain of eubacterial α subunit and forms a complex with Rpb3 subunit analogous to prokaryotic α2 homodimer, which is involved in RNA polymerase assembly and promoter recognition. In humans, a POLR2J gene family has been identified that potentially encodes several hRPB11 proteins differing mainly in their short C-terminal regions. The functions of the different human specific isoforms are still mainly unknown. To further characterize the minor human specific isoform of RNA polymerase II subunit hRPB11bα, the only one from hRPB11 (POLR2J) homologues that can replace its yeast counterpart in vivo, we used it as bait in a yeast two-hybrid screening of a human fetal brain cDNA library. By this analysis and subsequent co-purification assay in vitro, we identified transcription factor ATF4 as a prominent partner of the minor RNA polymerase II (RNAP II) subunit hRPB11bα. We demonstrated that the hRPB11bα interacts with leucine b-Zip domain located on the C-terminal part of ATF4. Overexpression of ATF4 activated the reporter more than 10-fold whereas co-transfection of hRPB11bα resulted in a 2.5-fold enhancement of ATF4 activation. Our data indicate that the mode of interaction of human RNAP II main (containing major for of hRPB11 subunit) and minor (containing hRPB11bα isoform of POLR2J subunit) transcription enzymes with ATF4 is certainly different in the two complexes involving hRPB3–ATF4 (not hRPB11a–ATF4) and hRpb11bα–ATF4 platforms in the first and the second case, respectively. The interaction of hRPB11bα and ATF4 appears to be necessary for the activation of RNA polymerase II containing the minor isoform of the hRPB11 subunit (POLR2J) on gene promoters regulated by this transcription factor. ATF4 activates transcription by directly contacting RNA polymerase II in the region of the heterodimer of α-like subunits (Rpb3–Rpb11) without involving a Mediator, which provides fast and highly effective activation of transcription of the desired genes. In RNA polymerase II of Homo sapiens that contains plural isoforms of the subunit hRPB11 (POLR2J), the strength of the hRPB11–ATF4 interaction appeared to be isoform-specific, providing the first functional distinction between the previously discovered human forms of the Rpb11 subunit.
Highlights
All messenger RNAs in eukaryotic cell are synthesized by RNA polymerase II (RNAPII), a complex enzyme, which consists of 12 subunits of the total weight over 0.8 MDa
We have shown that, in drastic difference with all other species, small indispensable subunit Rpb11 of RNA polymerase II is encoded in Homo sapiens by four different genes located on chromosome 7 [20,21]
It was previously described that human Rpb3 binds to transcription factors ATF4 [33] and myogenin [34], and that human Rpb11 interacts with Che-1 (AATF) [35]
Summary
All messenger RNAs in eukaryotic cell are synthesized by RNA polymerase II (RNAPII), a complex enzyme, which consists of 12 subunits of the total weight over 0.8 MDa. The overall structure of human RNAPII appears to be similar to the yeast one [1,2,3] as expected by the sequence conservation and the fact that a number of human subunits can functionally replace their yeast counterparts [13,14,15]. This was recently confirmed by 3D structure of mammalian (bovine) RNAPII with 3.4 Å resolution obtained by cryoelectron microscopy [6]. Despite high sequence and structure similarity to yeast RNAPII, there are likely unique features associated with the increased complexity of human RNAPII transcription system
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