<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Angelis KJ</submitter><funding>Czech Science Foundation</funding><pagination>1091</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12469541</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(9)</volume><pubmed_abstract>&lt;b>Background/Objectives&lt;/b>: The Structural Maintenance of Chromosomes (SMC) proteins form essential heterocomplexes for the preservation of DNA structure and its functions, and hence cell viability. The SMC5/6 dimer is assembled by direct interactions of ATP heads via the kleisin NSE4 bridge and by SMC hinges. The structure might be interrupted by a single point mutation within a conserved motif of the SMC6-hinge. We describe the phenomena associated with the impairment of the SMC5/6 complex with morphology, repair of DNA double strand breaks (DSB), mutagenesis, recombination and gene targeting (GT) in the moss &lt;i>Physcomitrium patens&lt;/i> (&lt;i>P. patens&lt;/i>). &lt;b>Methods&lt;/b>: Using CRISPR/Cas9-directed oligonucleotide replacement, we have introduced two close G to R point mutations in the </pubmed_abstract><journal>Genes</journal><pubmed_title>The Phenotype of &amp;lt;i&amp;gt;Physcomitrium patens SMC6&amp;lt;/i&amp;gt; Mutant with Interrupted Hinge Interactions.</pubmed_title><pmcid>PMC12469541</pmcid><funding_grant_id>GA23-05284S)</funding_grant_id><funding_grant_id>GA20-05095S</funding_grant_id><pubmed_authors>Hola M</pubmed_authors><pubmed_authors>Palecek JJ</pubmed_authors><pubmed_authors>Angelis KJ</pubmed_authors><pubmed_authors>Vaculikova J</pubmed_authors><pubmed_authors>Vagnerova R</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Phenotype of &amp;lt;i&amp;gt;Physcomitrium patens SMC6&amp;lt;/i&amp;gt; Mutant with Interrupted Hinge Interactions.</name><description>&lt;b>Background/Objectives&lt;/b>: The Structural Maintenance of Chromosomes (SMC) proteins form essential heterocomplexes for the preservation of DNA structure and its functions, and hence cell viability. The SMC5/6 dimer is assembled by direct interactions of ATP heads via the kleisin NSE4 bridge and by SMC hinges. The structure might be interrupted by a single point mutation within a conserved motif of the SMC6-hinge. We describe the phenomena associated with the impairment of the SMC5/6 complex with morphology, repair of DNA double strand breaks (DSB), mutagenesis, recombination and gene targeting (GT) in the moss &lt;i>Physcomitrium patens&lt;/i> (&lt;i>P. patens&lt;/i>). &lt;b>Methods&lt;/b>: Using CRISPR/Cas9-directed oligonucleotide replacement, we have introduced two close G to R point mutations in the </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Sep</publication><modification>2026-05-02T03:16:11.797Z</modification><creation>2026-05-02T03:11:11.423Z</creation></dates><accession>S-EPMC12469541</accession><cross_references><pubmed>41010035</pubmed><doi>10.3390/genes16091091</doi></cross_references></HashMap>