نتایج جستجو برای: evolving enhancer protein

تعداد نتایج: 1295154  

Journal: :The Journal of biological chemistry 2003
Zhihong Jiang Hao Tang Necat Havlioglu Xiaochun Zhang Stefan Stamm Riqiang Yan Jane Y Wu

Mutations in the human tau gene leading to aberrant splicing have been identified in FTDP-17, an autosomal dominant hereditary neurodegenerative disorder. Molecular mechanisms by which such mutations cause tau aberrant splicing were not understood. We characterized two mutations in exon 10 of the tau gene, N279K and Del280K. Our results revealed an exonic splicing enhancer element located in ex...

2004
Oliver Stoss Peter Stoilov Rosette Daoud Annette M. Hartmann Manuela Olbrich Stefan Stamm

Abbreviat ions : adrenocorticotrophic hormone, (ACTH); casein kinase I, (CKI); Cdc2-like kinase, (Clk); Concanavalin A, (ConA); cystic fibrosis transmembrane conductance regulator, (CFTR); epidermal growth factor, (EGF); exonic splicing enhancer, (ESE); exonic splicing silencer, (ESS); fibroblast growth factor, (FGF); heterogeneous nuclear protein, (hnRNP); interferon, (IFN); interleukin, (IL);...

2013
Altaf Hossain

For centuries, humankind accepts truth to be something static and global but Nietzsche has famously argued that truth is a metaphor and for that matter changeable and perennially evolving. As I hope to show here, this radical view has resulted out of Nietzsche’s meta-commentary on language and logic. The main purpose of this article is to examine the key points of Nietzsche’s arguments and the ...

2015
Kamesh Narasimhan Shubhadra Pillay Yong-Heng Huang Sriram Jayabal Barath Udayasuryan Veeramohan Veerapandian Prasanna Kolatkar Vlad Cojocaru Konstantin Pervushin Ralf Jauch

Sox2 and Pax6 are transcription factors that direct cell fate decision during neurogenesis, yet the mechanism behind how they cooperate on enhancer DNA elements and regulate gene expression is unclear. By systematically interrogating Sox2 and Pax6 interaction on minimal enhancer elements, we found that cooperative DNA recognition relies on combinatorial nucleotide switches and precisely spaced,...

Journal: :The EMBO journal 1998
A Muto H Hoshino L Madisen N Yanai M Obinata H Karasuyama N Hayashi H Nakauchi M Yamamoto M Groudine K Igarashi

Maf family transcription factors are important regulators in various differentiation systems. Putative Maf recognition elements (MAREs) are found in the 3' enhancer region of the immunoglobulin heavy chain (IgH) gene. These elements are bound in B-cell extracts by a heterodimeric protein complex containing both Bach2 and a small Maf protein. Analysis of normal hematopoietic cells revealed that ...

Journal: :Cell 1995
James V. Falvo Dimitris Thanos Tom Maniatis

In this paper, we investigate DNA bending induced by proteins required for virus induction of the human interferon-beta (IFN beta) gene. We show that NF-kappa B-DNA complexes that are functionally distinct in the context of the IFN beta enhancer are also conformationally distinct and that two sites in the enhancer contain in-phase bends that are counteracted or reversed by the binding of NF-kap...

Journal: :The Journal of Cell Biology 1992
A Gow V L Friedrich R A Lazzarini

The DNA sequence between position +36 and -1907 of the murine myelin basic protein gene contains the enhancer and promoter elements necessary for abundant and cell specific expression in transgenic mice. Surprisingly, the pattern of expression promoted by this DNA fragment is a subset of that exhibited by the endogenous myelin basic protein (MBP) gene. Fusion genes prepared with this promoter/e...

Journal: :Molecular and cellular biology 1999
T D Schaal T Maniatis

Splicing enhancers are RNA sequences required for accurate splice site recognition and the control of alternative splicing. In this study, we used an in vitro selection procedure to identify and characterize novel RNA sequences capable of functioning as pre-mRNA splicing enhancers. Randomized 18-nucleotide RNA sequences were inserted downstream from a Drosophila doublesex pre-mRNA enhancer-depe...

Journal: :Human molecular genetics 2014
Walid D Fakhouri Fedik Rahimov Catia Attanasio Evelyn N Kouwenhoven Renata L Ferreira De Lima Temis Maria Felix Larissa Nitschke David Huver Julie Barrons Youssef A Kousa Elizabeth Leslie Len A Pennacchio Hans Van Bokhoven Axel Visel Huiqing Zhou Jeffrey C Murray Brian C Schutte

DNA variation in Interferon Regulatory Factor 6 (IRF6) causes Van der Woude syndrome (VWS), the most common syndromic form of cleft lip and palate (CLP). However, an etiologic variant in IRF6 has been found in only 70% of VWS families. To test whether DNA variants in regulatory elements cause VWS, we sequenced three conserved elements near IRF6 in 70 VWS families that lack an etiologic mutation...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید