(A) Schematic illustration of Mbnl1 isoforms (modified from Tabaglio and colleagues [35]). Exons 5 and 7 are the most frequently alternatively spliced exons. Created with Biorender.com. (B) RT-PCR of Mbnl1 isoforms from control and Fmr1-depleted cell. At right is quantification of band intensities of exons 5 and 7 and mean ± SD is shown (Student’s t test, **p Mbnl1 RNA expression between the genotypes. (C) MBNL1 isoforms in the cytoplasm and nucleus in control and Fmr1 knockdown cells. Lamin B1 and GAPDH served as makers for the nuclear and cytoplasmic fractions, respectively. Quantification of the upper and lower MBNL1 bands relative to Lamin B1 or GAPDH is indicated. Mean ± SD is shown (Student’s t test, *p Fmr1 depletion. Quantification ...
<p>(A) Schematic representation of FL-MBNL1 and its deletion mutants. The FL-MBNL1 has four zinc-fin...
The work describes the increase in size of nuclear MBNL1-containing foci upon cell-cycle exit in fi...
(A, B) Gene structures of MBNL1 and MBNL2, adapted from [1,11]. Boxes represent exons, numbered 1–10...
(A) Changes in alternative RNA splicing across categories. (B) Violin plots illustrating the distrib...
(A) Co-immunoprecipitation of Mbnl1, Ptbp1, hnRNPF, hnRNPQ, and Srsf5 RNAs with FMRP. IgG and Srsf5 ...
The figure shows the tissue type and frequency where specific exons in Mbnl1 RNA mis-spliced upon FM...
(A) Mbnl1, Mbnl2, Ptbp1, and Ptbp2 RNA levels (in Ct value) N2A cells. (B) RT-pPCR analyses and repr...
(A) Schematic of experiment. Created with BioRender.com. (B) qPCR showing depletion of Fmr1 followin...
Analysis of MBNL1-binding sites was conducted using data from MBNL1 RIP-seq, with binding sites high...
Fragile X syndrome (FXS) is a neurodevelopmental disorder that is often modeled in Fmr1 knockout mic...
(A) Western blot for SETD2, H3K36me3, H3, and FMRP in nuclear extracts of control and Fmr1-deficient...
International audienceMuscleblind-like-1 (MBNL1) is a splicing regulatory factor controlling the fet...
Fragile X syndrome (FXS) is a neurodevelopmental disorder that is often modeled in Fmr1 knockout mic...
(A) Schematic outline of the CRISPR/Cas9 editing procedure by which the (CTG)2600 repeat was excised...
Impaired expression of the FMR1 gene is responsible for the fragile X mental retardation syndrome. T...
<p>(A) Schematic representation of FL-MBNL1 and its deletion mutants. The FL-MBNL1 has four zinc-fin...
The work describes the increase in size of nuclear MBNL1-containing foci upon cell-cycle exit in fi...
(A, B) Gene structures of MBNL1 and MBNL2, adapted from [1,11]. Boxes represent exons, numbered 1–10...
(A) Changes in alternative RNA splicing across categories. (B) Violin plots illustrating the distrib...
(A) Co-immunoprecipitation of Mbnl1, Ptbp1, hnRNPF, hnRNPQ, and Srsf5 RNAs with FMRP. IgG and Srsf5 ...
The figure shows the tissue type and frequency where specific exons in Mbnl1 RNA mis-spliced upon FM...
(A) Mbnl1, Mbnl2, Ptbp1, and Ptbp2 RNA levels (in Ct value) N2A cells. (B) RT-pPCR analyses and repr...
(A) Schematic of experiment. Created with BioRender.com. (B) qPCR showing depletion of Fmr1 followin...
Analysis of MBNL1-binding sites was conducted using data from MBNL1 RIP-seq, with binding sites high...
Fragile X syndrome (FXS) is a neurodevelopmental disorder that is often modeled in Fmr1 knockout mic...
(A) Western blot for SETD2, H3K36me3, H3, and FMRP in nuclear extracts of control and Fmr1-deficient...
International audienceMuscleblind-like-1 (MBNL1) is a splicing regulatory factor controlling the fet...
Fragile X syndrome (FXS) is a neurodevelopmental disorder that is often modeled in Fmr1 knockout mic...
(A) Schematic outline of the CRISPR/Cas9 editing procedure by which the (CTG)2600 repeat was excised...
Impaired expression of the FMR1 gene is responsible for the fragile X mental retardation syndrome. T...
<p>(A) Schematic representation of FL-MBNL1 and its deletion mutants. The FL-MBNL1 has four zinc-fin...
The work describes the increase in size of nuclear MBNL1-containing foci upon cell-cycle exit in fi...
(A, B) Gene structures of MBNL1 and MBNL2, adapted from [1,11]. Boxes represent exons, numbered 1–10...