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June 2019

The long-range action of Wingless/Wnt at compartment boundaries is essential for the development of the adult intestinal epithelium and overlying visceral muscles. Overexpression of Notum, a Wingless inhibitor, in the epithelium at the midgut-hindgut boundary and the adjacent posterior midgut results in extensive breaks and branches in the overlying longitudinal muscles and loss of the striated banding pattern of circular muscles (image). Similar muscle defects result from Wingless tethering at the midgut-hindgut boundary. See Tian et al.

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Image Credit: Ai Tian.

Perspectives

Diffusion and function of Wnt ligands

Richard A. Stewart, Aravinda-Bharathi Ramakrishnan, Ken M. Cadigan

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Research Articles

Asymmetrical localization of Nup107-160 subcomplex components within the nuclear pore complex in fission yeast

Haruhiko Asakawa, Tomoko Kojidani, Hui-Ju Yang, Chizuru Ohtsuki, Hiroko Osakada, Atsushi Matsuda, Masaaki Iwamoto, Yuji Chikashige, Koji Nagao, Chikashi Obuse, Yasushi Hiraoka, Tokuko Haraguchi

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A mutation in the endonuclease domain of mouse MLH3 reveals novel roles for MutLγ during crossover formation in meiotic prophase I

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Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease

Carles Vilariño-Güell, Alexander Zimprich, Filippo Martinelli-Boneschi, Bruno Herculano, Zhe Wang, Fuencisla Matesanz, Elena Urcelay, Koen Vandenbroeck, Laura Leyva, Denis Gris, Charbel Massaad, Jacqueline A. Quandt, Anthony L. Traboulsee, Mary Encarnacion, Cecily Q. Bernales, Jordan Follett, Irene M. Yee, Maria G. Criscuoli, Angela Deutschländer, Eva M. Reinthaler, Tobias Zrzavy, Elisabetta Mascia, Andrea Zauli, Federica Esposito, Antonio Alcina, Guillermo Izquierdo, Laura Espino-Paisán, Jorge Mena, Alfredo Antigüedad, Patricia Urbaneja-Romero, Jesús Ortega-Pinazo, Weihong Song, A. Dessa Sadovnick

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Cyclophilin B control of lysine post-translational modifications of skin type I collagen

Masahiko Terajima, Yuki Taga, Wayne A. Cabral, Ying Liu, Masako Nagasawa, Noriko Sumida, Yukako Kayashima, Prashant Chandrasekaran, Lin Han, Nobuyo Maeda, Irina Perdivara, Shunji Hattori, Joan C. Marini, Mitsuo Yamauchi

Essential gene deletions producing gigantic bacteria

Jeannie Bailey, Julie Cass, Joe Gasper, Ngoc-Diep Ngo, Paul Wiggins, Colin Manoil

Genomic variation predicts adaptive evolutionary responses better than population bottleneck history

Michael Ørsted, Ary Anthony Hoffmann, Elsa Sverrisdóttir, Kåre Lehmann Nielsen, Torsten Nygaard Kristensen

Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2

Heli Tiensuu, Antti M. Haapalainen, Minna K. Karjalainen, Anu Pasanen, Johanna M. Huusko, Riitta Marttila, Marja Ojaniemi, Louis J. Muglia, Mikko Hallman, Mika Rämet

Essential long-range action of Wingless/Wnt in adult intestinal compartmentalization

Ai Tian, Deepesh Duwadi, Hassina Benchabane, Yashi Ahmed

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Genome-wide association study of multisite chronic pain in UK Biobank

Keira J. A. Johnston, Mark J. Adams, Barbara I. Nicholl, Joey Ward, Rona J. Strawbridge, Amy Ferguson, Andrew M. McIntosh, Mark E. S. Bailey, Daniel J. Smith

Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb

Lars G. Fritsche, Lauren J. Beesley, Peter VandeHaar, Robert B. Peng, Maxwell Salvatore, Matthew Zawistowski, Sarah A. Gagliano Taliun, Sayantan Das, Jonathon LeFaive, Erin O. Kaleba, Thomas T. Klumpner, Stephanie E. Moser, Victoria M. Blanc, Chad M. Brummett, Sachin Kheterpal, Gonçalo R. Abecasis, Stephen B. Gruber, Bhramar Mukherjee

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Locus suicide recombination actively occurs on the functionally rearranged IgH allele in B-cells from inflamed human lymphoid tissues

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Convergent genetic aberrations in murine and human T lineage acute lymphoblastic leukemias

Benjamin J. Huang, Anica M. Wandler, Lauren K. Meyer, Monique Dail, Anneleen Daemen, Deepak Sampath, Qing Li, Xinyue Wang, Jasmine C. Wong, Joy Nakitandwe, James R. Downing, Jinghui Zhang, Barry S. Taylor, Kevin Shannon

Genetic and functional data identifying Cd101 as a type 1 diabetes (T1D) susceptibility gene in nonobese diabetic (NOD) mice

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Time of day and network reprogramming during drought induced CAM photosynthesis in Sedum album

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The gene regulatory basis of genetic compensation during neural crest induction

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Regulation of ectopic heterochromatin-mediated epigenetic diversification by the JmjC family protein Epe1

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Hepatitis C virus leaves an epigenetic signature post cure of infection by direct-acting antivirals

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Crossover recombination and synapsis are linked by adjacent regions within the N terminus of the Zip1 synaptonemal complex protein

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Actin assembly and non-muscle myosin activity drive dendrite retraction in an UNC-6/Netrin dependent self-avoidance response

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DREF Genetically Counteracts Mi-2 and Caf1 to Regulate Adult Stem Cell Maintenance

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Host-dependent nitrogen recycling as a mechanism of symbiont control in Aiptasia

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Parallel evolution leading to impaired biofilm formation in invasive Salmonella strains

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Congenital lipodystrophy induces severe osteosclerosis

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A Flp-SUMO hybrid recombinase reveals multi-layered copy number control of a selfish DNA element through post-translational modification

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miR-34 modulates wing polyphenism in planthopper

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Loss of ASAP1 in mice impairs adipogenic and osteogenic differentiation of mesenchymal progenitor cells through dysregulation of FAK/Src and AKT signaling

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Fasting prevents hypoxia-induced defects of proteostasis in C. elegans

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TDAG51 is a crucial regulator of maternal care and depressive-like behavior after parturition

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Correction

Correction: Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay

Olivier Duverger, Jenna C. Carlson, Chelsea M. Karacz, Mary E. Schwartz, Michael A. Cross, Mary L. Marazita, John R. Shaffer, Maria I. Morasso

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Opinion Piece

Solving the missing heritability problem

Alexander I. Young