Key Points• RHOA mutations are common in ATLL and show a unique distribution compared with other T-cell lymphomas.• Depending on patients, functionally distinct RHOA mutations are clonally selected and involved in the pathogenesis of ATLL.Adult T-cell leukemia/lymphoma (ATLL) is a distinct form of peripheral T-cell lymphoma with poor prognosis, which is caused by the human T-lymphotropic virus type 1 (HTLV-1). In contrast to the unequivocal importance of HTLV-1 infection in the pathogenesis of ATLL, the role of acquired mutations in HTLV-1 infected T cells has not been fully elucidated, with a handful of genes known to be recurrently mutated. In this study, we identified unique RHOA mutations in ATLL through whole genome sequencing of an index case, followed by deep sequencing of 203 ATLL samples. RHOA mutations showed distinct distribution and function from those found in other cancers. Involving 15% (30/203) of ATLL cases, RHOA mutations were widely distributed across the entire coding sequence but almost invariably located at the guanosine triphosphate (GTP)-binding pocket, with Cys16Arg being most frequently observed. Unexpectedly, depending on mutation types and positions, these RHOA mutants showed different or even opposite functional consequences in terms of GTP/guanosine diphosphate (GDP)-binding kinetics, regulation of actin fibers, and transcriptional activation. The Gly17Val mutant did not bind GTP/GDP and act as a dominant negative molecule, whereas other mutants (Cys16Arg and Ala161Pro) showed fast GTP/GDP cycling with enhanced transcriptional activation. These findings suggest that both loss-and gain-of-RHOA functions could be involved in ATLL leukemogenesis. In summary, our study not only provides a novel insight into the molecular pathogenesis of ATLL but also highlights a unique role of variegation of heterologous RHOA mutations in human cancers. (Blood. 2016;127(5):596-604)
Background: Di-Ras2 is a poorly characterized Ras-family GTPase specifically expressed in brain. Results: Di-Ras2 co-purifies with SmgGDS from cytosol, and the affinity of Di-Ras2 for guanine-nucleotides is reduced when complexed with SmgGDS. Conclusion: Di-Ras2 exits as a complex with SmgGDS in cytosol with lowered affinity for guanine nucleotides. Significance: Di-Ras2 activity may be atypically regulated by complex formation with SmgGDS.
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