Differential Translation of Dazap1 Transcripts during Spermatogenesis

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Differential Translation of Dazap1 Transcripts during Spermatogenesis

Deleted in AZoospermia Associated Protein 1 (DAZAP1) is a ubiquitous hnRNP protein that has been implicated in RNA transcription, splicing, and translation. It is highly expressed in testes, predominantly in late stage spermatocytes and post-meiotic spermatids. Dazap1 deficiency in mice results in growth retardation and spermatogenic arrest. The gene produces two major transcripts of 2.4 and 1....

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DAZAP1, an RNA-binding protein required for development and spermatogenesis, can regulate mRNA translation.

DAZ-associated protein 1 (DAZAP1) is an RNA-binding protein required for normal growth, development, and fertility in mice. However, its molecular functions have not been elucidated. Here we find that Xenopus laevis and human DAZAP1, which are each expressed as short and long forms, act as mRNA-specific activators of translation in a manner that is sensitive to the number of binding sites prese...

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DAZAP1 regulates the splicing of Crem, Crisp2 and Pot1a transcripts

Deleted in Azoospermia Associated Protein 1 (DAZAP1) is a ubiquitous heterogeneous nuclear ribonucleoprotein (hnRNP) that is expressed abundantly in the testis. DAZAP1 deficiency in mice results in growth retardation and spermatogenic arrest. Previous reports on DAZAP1's binding to several naturally occurring splicing mutations support a role for DAZAP1 in RNA splicing. To elucidate the biologi...

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The Use of Machine-Generated Transcripts During Human Translation

At the request of the USG National Virtual Translation Center, the University of Maryland Center for Advanced Study of Language conducted a study that assessed the role of several factors mediating transcript usefulness during translation tasks. These factors included source language (Mandarin or Modern Standard Arabic), native speaker status of the translators, transcript quality (low or moder...

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Differential histone modifications mark mouse imprinting control regions during spermatogenesis.

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ژورنال

عنوان ژورنال: PLoS ONE

سال: 2013

ISSN: 1932-6203

DOI: 10.1371/journal.pone.0060873