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Yoshimura, R.

Publications and source records attributed to Yoshimura, R..

2 recordsLinked to original sources

Direct Relationship between Protein Expression and Progeny Yield of Herpes Simplex Virus 1 Unveils a Rate-limiting Step for Virus Production

Although viral protein expression and progeny virus production were independently shown to be highly heterogenous in individual cells, their direct relationship, analyzed by considering their heterogeneities, has not been investigated to date. This study established a system to fractionate cells infected with a herpesvirus based on the levels of the global expression of viral late proteins, which are largely virion structural proteins, and to titrate virus yields in these fractions. This system demonstrated a direct relationship and indicated there was a threshold for the levels of viral late protein expression for progeny virus production and suggested that viral DNA cleavage/packaging was a rate-limiting step for progeny virus production. These findings, which were masked in previous studies performed at the entire population level, have uncovered a sophisticated viral strategy for efficient progeny virus production and shed new light on an effective target for the development of anti-viral drugs.

microbiology↗

The CRL plastid outer envelope protein supports TOC75-V / OEP80 complex formation in Arabidopsis

Embedded {beta}-barrel proteins in the outer envelope membrane mediate most cellular traffic between the cytoplasm and the plastids. Although TOC75-V/OEP80 has been implicated in the insertion and assembly of {beta}-barrel proteins in the outer envelope membrane of Arabidopsis thaliana, relatively little is known about this process. CRUMPLED LEAF (CRL) encodes a protein localizing in the outer envelope membrane, and its loss of function results in pleiotropic defects, including altered plant morphogenesis, growth retardation, suppression of plastid division, and spontaneous light intensity-dependent localized cell death. A suppressor screen conducted on mutagenized crl mutants with ethyl methanesulfonate revealed that a missense mutation in OEP80 suppresses crls pleiotropic defects. Furthermore, we found that the complex formation of OEP80 was compromised in crl. Furthermore, we demonstrated that CRL interacts with OEP80 in vivo and that a portion of CRL is present in protein complexes with the same molecular weight as the OEP80-associated complex. Our results suggest that CRL interacts with OEP80 to regulate its complex formation. CRL has been shown to be involved in plastid protein import; therefore, pleiotropic defects in crl are likely due to the combined effects of decreased plastid protein import and altered membrane integration of {beta}-barrel proteins in the outer envelope membrane. This study sheds light on the mechanisms that allow the integration of {beta}-barrel proteins into the outer envelope membrane of plastids and the significance of this finding for plant cellular processes.

plant biology↗