<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(1)</volume><submitter>Morimoto K</submitter><pubmed_abstract>F1 hybrid progenies between related subspecies often show hybrid sterility (HS) or inviability. HS is caused by failure of meiotic chromosome synapsis and sex body formation in house mouse. Previous studies identified two HS critical genomic regions named Hstx2 on Chr X and Hst1 on Chr 17 by murine forward genetic approaches. HS gene on Hst1 was reported to be Prdm9. Intersubspecific polymorphisms of Prdm9 induce HS in hybrids, and Prdm9 null mutation leads to sterility in the inbred strain. However, HS gene on Hstx2 remains unknown. Here, using knock-out studies, we showed that HS candidate genes on Hstx2 are not individually essential for spermatogenesis in B6 strain. We examined 12 genes on Hstx2: Ctag2, 4930447F04Rik, Mir743, Mir465d, Mir465c-2, Mir465b-1, Mir465c-1, Mir465, Gm1140, Gm</pubmed_abstract><journal>Scientific reports</journal><pagination>9060</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7270182</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Reverse genetics reveals single gene of every candidate on Hybrid sterility, X Chromosome QTL 2 (Hstx2) are dispensable for spermatogenesis.</pubmed_title><pmcid>PMC7270182</pmcid><pubmed_authors>Daitoku Y</pubmed_authors><pubmed_authors>Sugiyama F</pubmed_authors><pubmed_authors>Murata K</pubmed_authors><pubmed_authors>Morimoto K</pubmed_authors><pubmed_authors>Ayabe S</pubmed_authors><pubmed_authors>Kobayashi K</pubmed_authors><pubmed_authors>Suzuki H</pubmed_authors><pubmed_authors>Numata K</pubmed_authors><pubmed_authors>Hamada Y</pubmed_authors><pubmed_authors>Kato K</pubmed_authors><pubmed_authors>Takahashi S</pubmed_authors><pubmed_authors>Yoshiki A</pubmed_authors><pubmed_authors>Mizuno S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Reverse genetics reveals single gene of every candidate on Hybrid sterility, X Chromosome QTL 2 (Hstx2) are dispensable for spermatogenesis.</name><description>F1 hybrid progenies between related subspecies often show hybrid sterility (HS) or inviability. HS is caused by failure of meiotic chromosome synapsis and sex body formation in house mouse. Previous studies identified two HS critical genomic regions named Hstx2 on Chr X and Hst1 on Chr 17 by murine forward genetic approaches. HS gene on Hst1 was reported to be Prdm9. Intersubspecific polymorphisms of Prdm9 induce HS in hybrids, and Prdm9 null mutation leads to sterility in the inbred strain. However, HS gene on Hstx2 remains unknown. Here, using knock-out studies, we showed that HS candidate genes on Hstx2 are not individually essential for spermatogenesis in B6 strain. We examined 12 genes on Hstx2: Ctag2, 4930447F04Rik, Mir743, Mir465d, Mir465c-2, Mir465b-1, Mir465c-1, Mir465, Gm1140, Gm</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2025-04-04T11:22:49.388Z</modification><creation>2020-06-09T07:13:44Z</creation></dates><accession>S-EPMC7270182</accession><cross_references><pubmed>32493902</pubmed><doi>10.1038/s41598-020-65986-y</doi></cross_references></HashMap>