Target intelligence / Profile preview

Probable ATP-dependent RNA helicase DHX37 (DHX37)

Target
DHX37
Molecular classification
Enzyme, RNA helicase, DEAH-box family, ATPase
01

Overview

Probable ATP-dependent RNA helicase DHX37 (DHX37) is an enzyme belonging to the DEAH-box family of RNA helicases, characterized by conserved ATPase and RNA-binding domains. Its primary function is to facilitate the maturation of the small ribosomal subunit by catalyzing the unwinding of RNA secondary structures and the removal of U3 snoRNP from preribosomal particles during ribosome biogenesis. DHX37 contains a canonical DEAH ATPase/helicase core and a unique carboxy-terminal domain required for interaction with regulatory proteins such as UTP14A. It is expressed broadly, with crucial roles in early testis and brain development, and has been implicated in genetic diseases related to developmental anomalies and certain cancers. Disruption or mutation of DHX37 is associated with syndromes such as 46,XY sex reversal and neurodevelopmental disorders with brain anomalies[1][5][6][2].

Other names
DEAH-box helicase 37DDX37KIAA1517MGC4322Dhr1DEAH box protein 37DEAD/H box polypeptide 37DEAD/DEAH box helicase DDX37NEDBAVCSRXY11MGC2695putative ATP-dependent RNA helicase DHX37
02

Mechanism of action

ATP-dependent unwinding of RNA during ribosome assembly and pre-rRNA processing

03

Biological functions

Ribosome biogenesisRNA secondary structure unwindingRNA processing (including pre-rRNA processing)Regulation of gene expressionCellular growth and divisionEmbryogenesis and development
04

Disease associations

Genetic disorders including 46,XY sex reversal (SRXY11)Neurodevelopmental disorder with brain anomalies (NEDBAVC)Liver cancer and possibly other cancer types
05

Safety considerations

Not explicitly established as a therapeutic target, so specific safety concerns for direct inhibition/activation are unknownPotential essentiality for normal ribosome biogenesis and development may present a challenge for selective targeting
06

Biomarkers

Mutations in DHX37 have been associated with disorders of sex development and neurodevelopmental disorders, serving as genetic biomarkers in these contexts

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