<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhao L</submitter><funding>Natural Science Foundation of Beijing Municipality</funding><pagination>1563-1573</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6832345</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(1)</volume><pubmed_abstract>The episomal structures of all human bocavirus (HBoV) genotypes have been deciphered, including the circular genome of HBoV2 (HBoV2-C1). To discern the role of the circular HBoV2 genome, three distinct linearized HBoV2-C1 genomes were cloned into pBlueScript SKII(+) to obtain pBlueScript HBoV2 5043-5042 (retaining all secondary structures), pBlueScript-HBoV2 5075-5074 (retaining hairpin number 2 and the 5' terminal structure), and pBlueScript-HBoV2 5220-5219 (retaining only the 5' terminal structure at the 5' -genome end). The recombinant plasmids were separately transfected HEK293 cells, revealing that more HBoV2 DNA had accumulated in the pBlueScript HBoV2 5043-5042-transfected HEK293 cells at 72 h post-transfection, as determined by real-time PCR. However, more mRNA was transcribed by p</pubmed_abstract><journal>Emerging microbes &amp; infections</journal><pubmed_title>Keeping all secondary structures of the non-coding region in the circular genome of human bocavirus 2 is important for DNA replication and virus assembly, as revealed by three hetero-recombinant genomic clones.</pubmed_title><pmcid>PMC6832345</pmcid><funding_grant_id>7192029</funding_grant_id><pubmed_authors>Zhao L</pubmed_authors><pubmed_authors>Qian Y</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Dong H</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Zhu R</pubmed_authors><pubmed_authors>Jia L</pubmed_authors><pubmed_authors>Song J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Keeping all secondary structures of the non-coding region in the circular genome of human bocavirus 2 is important for DNA replication and virus assembly, as revealed by three hetero-recombinant genomic clones.</name><description>The episomal structures of all human bocavirus (HBoV) genotypes have been deciphered, including the circular genome of HBoV2 (HBoV2-C1). To discern the role of the circular HBoV2 genome, three distinct linearized HBoV2-C1 genomes were cloned into pBlueScript SKII(+) to obtain pBlueScript HBoV2 5043-5042 (retaining all secondary structures), pBlueScript-HBoV2 5075-5074 (retaining hairpin number 2 and the 5' terminal structure), and pBlueScript-HBoV2 5220-5219 (retaining only the 5' terminal structure at the 5' -genome end). The recombinant plasmids were separately transfected HEK293 cells, revealing that more HBoV2 DNA had accumulated in the pBlueScript HBoV2 5043-5042-transfected HEK293 cells at 72 h post-transfection, as determined by real-time PCR. However, more mRNA was transcribed by p</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2026-05-03T20:56:00.912Z</modification><creation>2020-05-21T18:36:32Z</creation></dates><accession>S-EPMC6832345</accession><cross_references><pubmed>31672101</pubmed><doi>10.1080/22221751.2019.1682949</doi></cross_references></HashMap>