Proteins interacting with (A) RHA/Mle, (B) DP103 and (C) p68/Dbp2, and the cellular processes in which they are involved, as examples to illustrate the multifunctional properties of the DExD/H box proteins discussed in this review. RHA has also been shown to interact with the promoters of the MDR1 and p16^INK4A genes; therefore these are also indicated.

A schematic alignment of the human homologues of the DExD/H box proteins considered in this review, highlighting the different lengths of the divergent N- and C-terminal domains. The conserved helicase cores [in yellow for DExH and light blue for DEAD (DEVD in the case of Ddx21)] are shown, with the conserved motifs within them numbered (I–VI) and highlighted in dark blue. The number of amino acids in the helicase cores and the N- and C-terminal domains are indicated for each protein. The functions of the conserved motifs are as follows: Motifs Q, I, II and VI are required for ATP binding and hydrolysis; motifs Ia, Ib, III, IV and V are thought to be involved in RNA binding. These are described more fully in the contribution by Linder (2,3). The accession numbers for these proteins are Dhx9- Q08211, Ddx20- Q9UH16, Ddx5- P17844, Ddx17- Q92841, Ddx21- Q9NR30 and Ddx54- Q8TDD1.

Models for mechanisms by which DExD/H box proteins, such as RHA and p68/p72, could recruit components of the transcription machinery to promoters or stabilize transcription initiation by acting as adaptor molecules or bridging factors, as suggested by the literature. Solid arrows indicate interactions documented in the literature; heavy dashed arrows are bridging roles suggested from the known interactions; faint dashed arrows with query marks are implied recruiting or bridging roles. (A) RHA through its interaction with CBP, RNA Pol II and BRCA1 has been suggested to act as a bridge between CBP and RNA Pol II and between BRCA1 and RNA Pol II. Since BRCA1 also interacts with other transcriptional regulators its interaction with RHA could facilitate in recruitment of RNA Pol II and other factors to the initiation complex or stabilize the initiation complex. (B) p68/p72 is known to interact with the AF1 domain of ERα and p68 has been shown to interact with CBP and RNA Pol II, leading to the suggestion that p68/p72 may act as bridges between the ERα AF1 domain and transcription factors interacting with the AF2 domain of ERα. p68/p72 could thus also enhance transcriptional activity by recruiting RNA Pol II to the initiation complex or by stabilizing the complex.