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Science

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Institución detectada Período Navegá Descargá Solicitá
No detectada desde mar. 1997 / hasta dic. 2023 Science Journals

Información

Tipo de recurso:

revistas

ISSN impreso

0036-8075

ISSN electrónico

1095-9203

Editor responsable

American Association for the Advancement of Science (AAAS)

País de edición

Estados Unidos

Fecha de publicación

Cobertura temática

Tabla de contenidos

Bills to give NSF massive spending boost advance in Senate and House, but hurdles remain

Jeffrey Mervis

Palabras clave: Multidisciplinary.

Pp. No disponible

A new twist on pasta dough could reshape food manufacturing

Joel Goldberg

Palabras clave: Multidisciplinary.

Pp. No disponible

An old antidepressant helps the immune system fight tumors in mice

Jocelyn Kaiser

Palabras clave: Multidisciplinary.

Pp. No disponible

Mammals can breathe through their intestines

Nikk Ogasa

Palabras clave: Multidisciplinary.

Pp. No disponible

Scientists tracking coronavirus variants struggle with global blind spots

Meredith Wadman

Palabras clave: Multidisciplinary.

Pp. No disponible

Erratum for the Report “Electrophotocatalytic diamination of vicinal C–H bonds,” by T. Shen and T. H. Lambert

Palabras clave: Multidisciplinary.

Pp. No disponible

Arene diversification through distal C(sp 2 )−H functionalization

Uttam DuttaORCID; Sudip Maiti; Trisha Bhattacharya; Debabrata MaitiORCID

<jats:title>Targeting distal C–H bonds in arenes</jats:title> <jats:p> The Friedel-Crafts reaction is among the oldest in organic chemistry. For well over a century, chemists have relied on electronic effects intrinsic to aryl rings to append substituents at specific sites along the periphery. However, only in the past decade have they devised catalytic techniques that over-ride these preferences so that new groups usually drawn to the neighboring sites of an existing substituent instead wind up two or three carbons away. Dutta <jats:italic>et al.</jats:italic> review progress in this field, highlighting elaborate directing groups and mediators as well as sophisticated ligand design. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" related-article-type="in-this-issue" xlink:href="10.1126/science.abd5992">eabd5992</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

SLFN2 protection of tRNAs from stress-induced cleavage is essential for T cell–mediated immunity

Tao YueORCID; Xiaoming ZhanORCID; Duanwu ZhangORCID; Ruchi JainORCID; Kuan-wen Wang; Jin Huk ChoiORCID; Takuma Misawa; Lijing SuORCID; Jiexia Quan; Sara HildebrandORCID; Darui XuORCID; Xiaohong LiORCID; Emre TurerORCID; Lei SunORCID; Eva Marie Y. MorescoORCID; Bruce BeutlerORCID

<jats:title>A T cell sleeper agent against stress</jats:title> <jats:p> Considerable changes in cellular metabolism occur when T cells transition from a resting to an activated state. One side effect of this process is an increase in reactive oxygen species (ROS). These molecules potentiate T cell receptor (TCR) signaling but can also result in detrimental oxidative stress (see the Perspective by Su and Dutta). Yue <jats:italic>et al.</jats:italic> describe one mechanism by which T cells can resolve this contradiction. Using mice with a T cell-specific deficiency in Schlafen 2 (SLFN2), they found that this protein binds to and protects transfer RNAs from oxidative stress-induced cleavage by the ribonuclease angiogenin. This process is downstream of ROS generation, which allows activated T cells to maintain protein synthesis despite the ROS that would otherwise inhibit translation. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" related-article-type="in-this-issue" xlink:href="10.1126/science.aba4220">eaba4220</jats:related-article> ; see also p. <jats:related-article issue="6543" page="683" related-article-type="in-this-issue" vol="372">683</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

A prometastatic splicing program regulated by SNRPA1 interactions with structured RNA elements

Lisa FishORCID; Matvei KhoroshkinORCID; Albertas NavickasORCID; Kristle Garcia; Bruce Culbertson; Benjamin Hänisch; Steven Zhang; Hoang C. B. NguyenORCID; Larisa M. SotoORCID; Maria DermitORCID; Faraz K. MardakhehORCID; Henrik MolinaORCID; Claudio AlarcónORCID; Hamed S. NajafabadiORCID; Hani GoodarziORCID

<jats:title>Characterizing a cancer spliceosome</jats:title> <jats:p> Cells undergo many genomic changes as they progress toward metastatic cancer. One aspect of this change is to RNA expression and splicing isoforms, but how these differences affect tumor progression is not well characterized. Fish <jats:italic>et al.</jats:italic> developed a computational framework called pyTEISER that identifies structural cis-regulatory elements that control diverse types of RNA regulation. Applying pyTEISER to models of breast cancer metastasis, they discovered an RNA short-stem-loop element that forms a “structural splicing enhancer” that acts in cis to regulate alternative splicing of RNA transcripts. One of these interactions encompasses the RNA-binding protein SNRPA1 and results in alternative exon inclusion that affects metastatic capacity in xenograft models. Thus, RNA element binding may play a role in splicing regulation and is potentially an important component of the cis-splicing code. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" related-article-type="in-this-issue" xlink:href="10.1126/science.abc7531">eabc7531</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

A cell type–specific cortico-subcortical brain circuit for investigatory and novelty-seeking behavior

Mehran AhmadlouORCID; Janou H. W. HoubaORCID; Jacqueline F. M. van VierbergenORCID; Maria GiannouliORCID; Geoffrey-Alexander Gimenez; Christiaan van Weeghel; Maryam DarbanfouladiORCID; Maryam Yasamin ShiraziORCID; Julia DziubekORCID; Mejdy KacemORCID; Fred de WinterORCID; J. Alexander HeimelORCID

<jats:title>A brain circuit that drives and gates curiosity</jats:title> <jats:p> Curiosity is what drives organisms to investigate each other and their environment. It is considered by many to be as intrinsic as hunger and thirst, but the neurobiological mechanisms behind curiosity have remained elusive. In mice, Ahmadlou <jats:italic>et al.</jats:italic> found that a specific population of genetically identified γ-aminobutyric acid (GABA)—ergic neurons in a brain region called the zona incerta receive excitatory input in the form of novelty and/or arousal information from the prelimbic cortex, and these neurons send inhibitory projections to the periaqueductal gray region (see the Perspective by Farahbakhsh and Siciliano). This circuitry is necessary for the exploration of new objects and conspecifics. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" related-article-type="in-this-issue" xlink:href="10.1126/science.abe9681">eabe9681</jats:related-article> ; see also p. <jats:related-article issue="6543" page="684" related-article-type="in-this-issue" vol="372">684</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible