DHH1 cDNA ORF clone, Saccharomyces cerevisiae S288C

The nucleotide sequence of Saccharomyces cerevisiae chromosome IV.
Jacq C, Alt-M?rbe J, Andre B, Arnold W, Bahr A, Ballesta JP, Bargues M, Baron L, Becker A, Biteau N, Bl?cker H, Blugeon C, Boskovic J, Brandt P, Br?ckner M, Buitrago MJ, Coster F, Delaveau T, del Rey F, Dujon B, Eide LG, Garcia-Cantalejo JM, Goffeau A, Gomez-Peris A, Zaccaria P
Nature387(6632 Suppl)75-8(1997 May)

Life with 6000 genes.
Goffeau A, Barrell BG, Bussey H, Davis RW, Dujon B, Feldmann H, Galibert F, Hoheisel JD, Jacq C, Johnston M, Louis EJ, Mewes HW, Murakami Y, Philippsen P, Tettelin H, Oliver SG
Science (New York, N.Y.)274(5287)546, 563-7(1996 Oct)

These results suggest that after localization to the bud tip, a portion of the localized ASH1 mRNA becomes translationally inactive because of binding of Dhh1 and Puf6 to the 5'- and 3'-UTRs of ASH1 mRNA.
Title: Binding of DEAD-box helicase Dhh1 to the 5'-untranslated region of

findings show that the mutations in ATPase A and B motif (K96R, D195A) affected the growth at non-permissive temperature, the mating processes including the Ste12 expression, and the P-body accumulation
Title: Mutational analysis of the RNA helicase Dhh1 in Ste12 expression and yeast mating.

All Dhh1-dependent mRNAs, viral and cellular, share key common features. First, they contain long and highly structured CDSs, including a region located around nucleotide 70 after the translation initiation site; second, they are directly bound by Dhh1 with a specific binding distribution; and third, complementary experimental approaches suggest that they are activated by Dhh1 at the translation initiation step
Title: A novel translational control mechanism involving RNA structures within coding sequences.

Here, the authors show that in budding yeast, mutations in the DEAD-box ATPase Dhh1 that prevent ATP hydrolysis, or that affect the interaction between Dhh1 and Not1, the central scaffold of the CCR4-NOT complex and an activator of the Dhh1 ATPase, prevent processing bodies disassembly in vivo.
Title: ATPase activity of the DEAD-box protein Dhh1 controls processing body formation.

Data indicate that RNA helicase RCK family member Dhh1 and the mRNA decay pathway coordinately repress the autophagy gene expression.
Title: A conserved mechanism of TOR-dependent RCK-mediated mRNA degradation regulates autophagy.