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Xenopus laevis

ABSTRACT: miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones

PROVIDER: PRJNA148701 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR360852.fastq.gz	Fastqsanger.gz
	SRR360853.fastq.gz	Fastqsanger.gz
	SRR360854.fastq.gz	Fastqsanger.gz
	SRR360855.fastq.gz	Fastqsanger.gz
	SRR360856.fastq.gz	Fastqsanger.gz

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Similar Datasets

miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones

Project description:During axon pathfinding, growth cones commonly exhibit changes in sensitivity to guidance cues that follow a strict timetable, even in the absence of pathway feedback, implicating cell-intrinsic regulation. Cellular timer mechanisms, however, are poorly understood. Here we have investigated microRNAs in the timing control of Sema3A sensitivity in retinal ganglion cell (RGC) growth cones. A developmental profiling screen identified miR-124 as a candidate timer. Loss of miR-124 delayed the onset of Sema3A sensitivity and concomitant Neuropilin-1 (NRP-1) receptor expression, and caused cell autonomous pathfinding errors. CoREST, a cofactor of a NRP1 repressor, was identified as a novel target and mediator of miR-124 for this highly specific temporal aspect of RGC growth cone responsiveness. Our findings indicate that miR-124 plays an important role in regulating the intrinsic temporal changes in RGC growth cone sensitivity and suggest that microRNAs may play a broad role as linear timers in vertebrate neuronal development. Two independent experiments were performed. One with a single sample for each of 3 stages, and the second with 2 biological replicates of each stage.

2011-12-12 | E-GEOD-33444 | biostudies-arrayexpress

miR-124 acts through coREST to control the onset of Sema3A sensitivity in navigating retinal growth cones

2011-12-12 | GSE33444 | GEO

Xenopus laevis

Project description:Translational profiling of retinal ganglion cell optic nerve regeneration in Xenopus laevis

| PRJNA311315 | ENA

Subcellular expression profiling of the growth cones of retinal ganglion cells (RGC)

Project description:Cue-directed axon guidance depends partly on local translation in growth cones. Many mRNA transcripts are known to reside in developing axons yet little is known about their subcellular distribution or, specifically, which transcripts are in growth cones. Laser capture microdissection (LCM) was used to isolate the growth cones of retinal ganglion cell (RGC) axons of two vertebrate species, mouse and Xenopus, coupled with unbiased genome-wide microarray profiling. Localized mRNA from the isolated growth cones of Xenopus laevis and Mus musculus retinal ganglion cells were subjected to microarray analysis

2010-11-23 | E-GEOD-25166 | biostudies-arrayexpress

Gene expression in sexually differentiating gonads of Xenopus laevis

Project description:The aim of this study was to study the gene expression profile in developing female and male gonads of Xenopus laevis at four stages: at the Nieuwkoop-Faber stage 50 (genital ridge), at NF53 (sex-determining period), NF56 (the onset of sexual differentiation), NF62 (gonads sexually differentiated).

2017-10-18 | GSE105103 | GEO

Generation and Care of Xenopus laevis and Xenopus tropicalis Embryos.

Project description:Robust and efficient protocols for fertilization and early embryo care of Xenopus laevis and Xenopus tropicalis are essential for experimental success, as well as maintenance and propagation of precious animal stocks. The rapid growth of the National Xenopus Resource has required effective implementation and optimization of these protocols. Here, we discuss the procedures used at the National Xenopus Resource, which we found helpful for generation and early upkeep of Xenopus embryos and tadpoles.

| S-EPMC6396978 | biostudies-literature

Xenopus laevis laevis

Project description:Xenopus laevis Developing Eye Transcriptomes

| PRJNA1124041 | ENA

Xenopus laevis laevis

Project description:Xenopus laevis Transcriptome or Gene expression

| PRJNA255991 | ENA

Xenopus laevis laevis

Project description:Xenopus laevis laevis Transcriptome or Gene expression

| PRJNA247381 | ENA

Evolutionary divergence in tail regeneration between Xenopus laevis and Xenopus tropicalis.

Project description:Tissue regeneration is of fast growing importance in the development of biomedicine, particularly organ replacement therapies. Unfortunately, many human organs cannot regenerate. Anuran Xenopus laevis has been used as a model to study regeneration as many tadpole organs can regenerate. In particular, the tail, which consists of many axial and paraxial tissues, such as spinal cord, dorsal aorta and muscle, commonly present in vertebrates, can fully regenerate when amputated at late embryonic stages and most of the tadpole stages. Interestingly, between stage 45 when feeding begins to stage 47, the Xenopus laevis tail cannot regenerate after amputation. This period, termed "refractory period", has been known for about 20 years. The underlying molecular and genetic basis is unclear in part due to the difficult to carry out genetic studies in this pseudo-tetraploid species. Here we compared tail regeneration between Xenopus laevis and the highly related diploid anuran Xenopus tropicalis and found surprisingly that Xenopus tropicalis lacks the refractory period. Further molecular and genetic studies, more feasible in this diploid species, should reveal the basis for this evolutionary divergence in tail regeneration between two related species and facilitate the understanding how tissue regenerative capacity is controlled, thus with important implications for human regenerative medicine.

| S-EPMC8028753 | biostudies-literature

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