Table of Contents

May 1, 2021; 35 (9-10)

REVIEWS

  • In this review, Klein et al. discuss the p53-independent roles of MDM2 and MDMX. First, they review the structural and functional features of MDM2 and MDMX proteins separately and together that could be relevant to their p53-independent activities. Following this, they summarize how these two proteins are regulated and how they can function in cells that lack p53.

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    In this review, Pilger et al. summarize the current understanding of the molecular mechanisms underlying DNA damage-triggered immune responses, including cytosolic DNA sensing via the cGAS/STING pathway. They also highlight the implications of DDR components for therapeutic outcomes of immune checkpoint inhibitors or their use as biomarkers.

  • OPEN ACCESS ARTICLE

    In this review, Frost et al. summarize the current knowledge on the Cip/Kip family of cyclin-dependent kinase inhibitors in mouse gonad development and highlight new roles for cell cycle inhibitors in controlling and maintaining female fertility.

  • In this review, Bideyan et al. summarize the advances in our understanding of the gene regulatory networks that contribute to hepatic responses to fasting and feeding. They also discuss how dietary modifications modulate hepatic gene expression programs.

  • In this review, Cossa et al. discuss the current knowledge and outstanding questions about phosphatases in the context of the RNAPII transcription cycle.

  • In this review, Choi et al. compare the spontaneous activity of the developing visual system between mammals and Drosophila and suggest that Drosophila is an emerging model for mechanistic and functional studies of correlated spontaneous activity.

RESEARCH COMMUNICATION

  • In this study, Ma et al. set out to study the mechanism of centromeric cohesion protection by Moa1/meikin during meiosis I. Using genetic and fluorescence microscopy approaches in fission yeast, the authors show that Moa1-Plo1 phosphorylates Rec8, which is required for Sgo1-PP2A to protect centromeric cohesion by antagonizing CK1-mediated phosphorylation of the cohesion subunit Rec8.

RESEARCH PAPERS

  • Here, Viktorovskaya et al. sought to understand how the functions of three essential histone chaperones are coordinated during gene transcription. Using genetic and biochemical approaches, this work sheds light on previously unknown connections between FACT activity and the functions of Spt6 and Spn1.

  • In this study, Jang et al. investigated the role of MED1 in adipose development and expansion in vivo, and they show that MED1 is not generally required for transcription during adipogenesisin culture and that MED1 is dispensable for adipose development in mice. Instead, MED1 is required for postnatal adipose expansion and the induction of fatty acid and triglyceride synthesis genes after pups switch diet from high-fat maternal milk to carbohydrate-based chow. Their findings identify a cell- and gene-specific regulatory role of MED1 as a lipogenesis coactivator required for postnatal adipose expansion.

  • In this study, Ito et al. sought to understand the precise roles of MED1, and its various domains, at various stages of adipogenesis and in adipose tissue. Using multiple genetic approaches to assess requirements for MED1 in adipocyte formation and function in mice, they show that MED1 is indeed essential for the differentiation and/or function of both brown and white adipocytes, as its absence in these cells leads to, respectively, defective brown fat function and lipodystrophy.

  • Here, Fursova et al. investigated the role of BAP1, an H2AK119ub1 deubiquitylating enzyme, in regulating gene expression in mouse ESCs. Using inducible genetic perturbations and quantitative genomics, they show that BAP1 plays a widespread role in promoting gene expression and that this relies on BAP1 counteracting pervasive H2AK119ub1. In the absence of BAP1, accumulation of H2AK119ub1 throughout the genome leads to widespread reductions in transcription.

RESOURCE/METHODOLOGY

  • In this Resource/Methodology, O'Connor et al. performed high-throughput sequencing of RNA isolated by cross-linking immunoprecipitation (HITS-CLIP) to comprehensively characterize the network of high-confidence, in vivo mRNA:miRNA interactions across white and brown fat, revealing >27,000 unique AGO binding sites. Their work represents the only experimentally generated miRNA targetome in adipose tissue and identifies multiple regulatory pathways that may specify the unique identities of white and brown fat.

CORRIGENDA

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