Relevant bibliographies by topics / Utp25

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  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'Utp25'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Utp25"

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Charette, J. M., and S. J. Baserga. "The DEAD-box RNA helicase-like Utp25 is an SSU processome component." RNA 16, no. 11 (2010): 2156–69. http://dx.doi.org/10.1261/rna.2359810.

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2

Huang, Weidong, Feng Chen, Quanxin Ma, et al. "Ribosome biogenesis gene DEF/UTP25 is essential for liver homeostasis and regeneration." Science China Life Sciences 63, no. 11 (2020): 1651–64. http://dx.doi.org/10.1007/s11427-019-1635-2.

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3

Bernstein, Kara A., Jennifer E. G. Gallagher, Brianna M. Mitchell, Sander Granneman, and Susan J. Baserga. "The Small-Subunit Processome Is a Ribosome Assembly Intermediate." Eukaryotic Cell 3, no. 6 (2004): 1619–26. http://dx.doi.org/10.1128/ec.3.6.1619-1626.2004.

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ABSTRACT The small-subunit (SSU) processome is a large ribonucleoprotein required for the biogenesis of the 18S rRNA and likely corresponds to the terminal knobs visualized by electron microscopy on the 5′ end of nascent rRNAs. The original purification of the SSU processome of Saccharomyces cerevisiae resulted in the identification of 28 proteins. Here, we characterize 12 additional protein components, including five small-ribosomal-subunit proteins (Rps4, Rps6, Rps7, Rps9, and Rps14) that had previously been copurified. Our multiple criteria for including a component as a bona fide SSU proce
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4

Champion, Erica A., Bennett H. Lane, Meredith E. Jackrel, Lynne Regan, and Susan J. Baserga. "A Direct Interaction between the Utp6 Half-a-Tetratricopeptide Repeat Domain and a Specific Peptide in Utp21 Is Essential for Efficient Pre-rRNA Processing." Molecular and Cellular Biology 28, no. 21 (2008): 6547–56. http://dx.doi.org/10.1128/mcb.00906-08.

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ABSTRACT The small subunit (SSU) processome is a ribosome biogenesis intermediate that assembles from its subcomplexes onto the pre-18S rRNA with yet unknown order and structure. Here, we investigate the architecture of the UtpB subcomplex of the SSU processome, focusing on the interaction between the half-a-tetratricopeptide repeat (HAT) domain of Utp6 and a specific peptide in Utp21. We present a comprehensive map of the interactions within the UtpB subcomplex and further show that the N-terminal domain of Utp6 interacts with Utp18 while the HAT domain interacts with Utp21. Using a panel of
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5

Butterfield, Andrew. "UTP2: Higher-Order Equational Reasoning by Pointing." Electronic Proceedings in Theoretical Computer Science 167 (October 29, 2014): 14–22. http://dx.doi.org/10.4204/eptcs.167.4.

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6

Sato, Manae, Nanase Araki, Masahiro Kumeta, et al. "Interaction, mobility, and phosphorylation of human orthologues of WD repeat-containing components of the yeast SSU processome t-UTP sub-complex." Biochemistry and Cell Biology 91, no. 6 (2013): 466–75. http://dx.doi.org/10.1139/bcb-2013-0062.

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We previously proposed a dynamic scaffold model for inner nuclear structure formation. In this model, structures in inter-chromatin regions are maintained through dynamic interaction of protein complex modules, and WD repeat- and disordered region-rich proteins and others act as scaffolds for these protein complexes. In this study, three WD-repeat proteins, i.e., CIRH1A, UTP15, and WDR43, were found in the nuclear matrix fraction and speculated to be present in the human t-UTP sub-complex of SSU processomes. The results obtained as to their subnuclear localization, binding with each other, mob
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7

Rudra, Dipayan, Jaideep Mallick, Yu Zhao, and Jonathan R. Warner. "Potential Interface between Ribosomal Protein Production and Pre-rRNA Processing." Molecular and Cellular Biology 27, no. 13 (2007): 4815–24. http://dx.doi.org/10.1128/mcb.02062-06.

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ABSTRACT It has become clear that in Saccharomyces cerevisiae the transcription of ribosomal protein genes, which makes up a major proportion of the total transcription by RNA polymerase II, is controlled by the interaction of three transcription factors, Rap1, Fhl1, and Ifh1. Of these, only Rap1 binds directly to DNA and only Ifh1 is absent when transcription is repressed. We have examined further the nature of this interaction and find that Ifh1 is actually associated with at least two complexes. In addition to its association with Rap1 and Fhl1, Ifh1 forms a complex (CURI) with casein kinas
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8

Kong, RuiRui, Wei Han, H. Weidle Ulrich, Tao Ning, XiaoJuan Du, and Yang Ke. "1A6/DRIM, the human UTP20 functions in 28S and 5.8S rRNA processing." Chinese Science Bulletin 55, no. 17 (2010): 1770–76. http://dx.doi.org/10.1007/s11434-010-3166-8.

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9

Brickman, Timothy J., and Sandra K. Armstrong. "Bordetella Interspecies Allelic Variation in AlcR Inducer Requirements: Identification of a Critical Determinant of AlcR Inducer Responsiveness and Construction of an alcR(Con) Mutant Allele." Journal of Bacteriology 184, no. 6 (2002): 1530–39. http://dx.doi.org/10.1128/jb.184.6.1530-1539.2002.

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ABSTRACT Previous studies established the critical roles of AlcR and alcaligin inducer in positive regulation of alcaligin siderophore biosynthesis and transport genes in Bordetella pertussis and Bordetella bronchiseptica. Transcriptional analyses using plasmid-borne alcR genes of B. pertussis UT25 and B. bronchiseptica B013N to complement the alcR defect of B. bronchiseptica strain BRM13 (ΔalcR1 alcA::mini-Tn5 lacZ1) revealed interspecies differences in AlcR inducer requirements for activation of alcABCDER operon transcription. Whereas the B. pertussis UT25 AlcR protein retained strong induce
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10

An, Weidong, Yifei Du, and Keqiong Ye. "Structural and functional analysis of Utp24, an endonuclease for processing 18S ribosomal RNA." PLOS ONE 13, no. 4 (2018): e0195723. http://dx.doi.org/10.1371/journal.pone.0195723.

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Dissertations / Theses on the topic "Utp25"

1

Cruz, Ana Maria Martins Marques da. "Estudo das interações de Utp25 com outros componentes do complexo SSU processomo." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-14092016-093631/.

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A síntese de ribossomos é um dos principais processos celulares e na levedura Saccharomyces cerevisiae são necessários 75 snoRNAs e mais de 200 proteínas não-ribossomais para que o ribossomo seja corretamente formado. Para o processamento do precursor dos RNAs ribossomais, chamado pré-rRNA 35S, ocorre o pareamento deste com o U3 snoRNA e outros snoRNAs e diversas proteínas se associam de maneira orquestrada e transitória, formando o complexo SSU processomo. Tal complexo é necessário para o processamento da região 5\' do pré-rRNA 35S e para a correta montagem e maturação da subunidade menor rib
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Conference papers on the topic "Utp25"

1

Nakakuki, Makoto, Koki Abe, Hitoshi Ando, et al. "Proposal for Enhancing UTP2 with Test Aspects." In 2018 IEEE International Conference on Software Testing, Verification and Validation Workshops (ICSTW). IEEE, 2018. http://dx.doi.org/10.1109/icstw.2018.00059.

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