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   https://doi.org/10.1002/ehs2.1229  

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2. The long and short of the S ‐locus in Turnera (Passifloraceae)

   https://doi.org/10.1111/nph.15970  

   Shore, Joel S.; Hamam, Hasan J.; Chafe, Paul D. J.; Labonne, Jonathan D. J.; Henning, Paige M.; McCubbin, Andrew G. (July 2019, New Phytologist)

   Summary Distyly is an intriguing floral adaptation that increases pollen transfer precision and restricts inbreeding. It has been a model system in evolutionary biology since Darwin. Although theS‐locus determines the long‐ and short‐styled morphs, the genes were unknown inTurnera. We have now identified these genes.We used deletion mapping to identify, and then sequence,BACclones and genome scaffolds to constructS/shaplotypes. We investigated candidate gene expression, hemizygosity, and used mutants, to explore gene function.Thes‐haplotype possessed 21 genes collinear with a region of chromosome 7 of grape. TheS‐haplotype possessed three additional genes and two inversions.TsSPH1was expressed in filaments and anthers,TsYUC6in anthers andTsBAHDin pistils. Long‐homostyle mutants did not possessTsBAHDand a short‐homostyle mutant did not expressTsSPH1.Three hemizygous genes appear to determine S‐morph characteristics inT. subulata. Hemizygosity is common to all distylous species investigated, yet the genes differ. The pistil candidate gene,TsBAHD, differs from that ofPrimula, but both may inactivate brassinosteroids causing short styles.TsYUC6is involved in auxin synthesis and likely determines pollen characteristics.TsSPH1is likely involved in filament elongation. We propose an incompatibility mechanism involvingTsYUC6andTsBAHD. 

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3. The Gaia -ESO Survey: the origin and evolution of s -process elements

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   Magrini, L.; Spina, L.; Randich, S.; Friel, E.; Kordopatis, G.; Worley, C.; Pancino, E.; Bragaglia, A.; Donati, P.; Tautvaišienė, G.; et al (September 2018, Astronomy & Astrophysics)
4. Comparative Analysis of the Chloroplast Genomes of Quercus × morehus and the Presumptive Parents Q. wislizeni and Q. kelloggii (Fagaceae) from California

   https://doi.org/10.1128/mra.00321-22  

   Garcia, Alejandro; Katada, Althea C.; Serrano, Alyssa; Gonzalez-Karlsson, Adrea; Carrillo, Angel; Castellanos, Angelica; Mendez-Gomez, Azucena; Flores, Carlos J.; Limon, Christopher; Lopez, Cynthia; et al (July 2022, Microbiology Resource Announcements)

   Stajich, Jason E. (Ed.)

   ABSTRACT Here, we present the complete chloroplast genomes of Quercus × morehus , Q. wislizeni , and Q. kelloggii from California. The genomes are 161,119 to 161,130 bp and encode 132 genes. Quercus × morehus and Q. wislizeni are identical in sequence but differ from Q. kelloggii by three indels and eight SNPs. 

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   Centromeres attach chromosomes to spindle microtubules during cell division and, despite this conserved role, show paradoxically rapid evolution and are typified by complex repeats. We used long-read sequencing to generate the Col-CEN Arabidopsis thaliana genome assembly that resolves all five centromeres. The centromeres consist of megabase-scale tandemly repeated satellite arrays, which support CENTROMERE SPECIFIC HISTONE H3 (CENH3) occupancy and are densely DNA methylated, with satellite variants private to each chromosome. CENH3 preferentially occupies satellites that show the least amount of divergence and occur in higher-order repeats. The centromeres are invaded by ATHILA retrotransposons, which disrupt genetic and epigenetic organization. Centromeric crossover recombination is suppressed, yet low levels of meiotic DNA double-strand breaks occur that are regulated by DNA methylation. We propose that Arabidopsis centromeres are evolving through cycles of satellite homogenization and retrotransposon-driven diversification. 

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