Foxn4CR4.2-GFP Reporter Plasmid

This GFP reporter plasmid expresses Foxn4CR4.2, a noncoding sequence upstream of the Foxn4 locus.

Highlights:

  • Expresses Foxn4CR4.2 with GFP reporter.
  • Foxn4CR4.2 has been identified as a 129 bp DNA fragment of CR4, located approximately 50kb upstream of Foxn4 transcription start site.
  • CR4.2 functions as a novel cis-regulator that directs retinal cell type specific gene expression.
  • CR4.2 is preferentially active in the Foxn4 expressing cells.
  • The specific trans-acting factor Meis1 has been shown to interact with CR4.2 and is essiential for proper CR4.2 function.

Transcription factor forkhead box N4 (Foxn4) cooperates with key retinogenic factors to mediate the multipotent differentiation of retinal progenitors and is believed to regulate neuronal subtype diversification. FOXN4 is expressed in a subset of mitotic progenitors during retinogenesis. As such, Foxn4 controls the formation of amacrine and horizontal cells by activating the expression of the retinogenic factors MATH-3, Neuro D and PROX1. During spinal neurogenesis, the p2 progenitor domain gives rise to two intermingled distinct subtypes of interneurons, termed V2a and V2b. Foxn4 is coexpressed with the bHLH factor ASH1 (Mash1) in a subset of p2 progenitors. Functionality of Foxn4 affects ASH1 expression and regulates interneuronal formation accordingly. Over-expression of Foxn4 alone in spinal neural progenitors promotes the V2a fate at the expense of the V2b fate, whereas ASH1 suppresses both the V2a and V2b fates.

From the laboratory of Li Cai, PhD, Rutgers University.

The Investigator's Annexe Part of The Investigator's Annexe program.

Catalog Number Product Size AVAILABILITY Price Qty
ED4001
Foxn4CR4.2-GFP Reporter Plasmid
Spotted on filter paper In stock
Price: $68.00
Specifications
Product Type: Plasmid
Gene/insert name: Foxn4CR4.2 ? a noncoding sequence upstream of Foxn4 locus
Antibiotic Resistance: Ampicillin
Fusion Tag(s): GFP
Format: Liquid/spotted on filter paper
Grow in E. coli at 37 C: Yes
Selectable markers: GFP
Cloning Site 5': SpeI
Cloning Site 3': FseI
Insert Size: 129 bp
Vector Backbone and Size: basal beta-globin promoter (bGP-GFP)
High or low copy: High
Storage: -20C
Shipped: Ambient temperature
Data

CR4.2 directs GFP expression in Foxn4+ cells and differentiating horizontal cells.

Chick retinas were electroporated with either the control CAG-GFP construct or CR4.2-bGP-GFP (CR4.2-GFP) construct at embryonic day 4 (E4). Transfected retinas were harvested at E6, E7, and E8 during development, sectioned, and immunostained for GFP (green) and Foxn4 (red). Double labeled cells (boxed regions) are shown in highermagnification on the right (indicated by arrowheads; arrows point to Foxn4-negative cells). Scale bar: 20 mm.

Adapted from: Islam MM, et al. Biol Open. 2013 Sep 6;2(11):1125-36.

Provider
From the laboratory of Li Cai, PhD, Rutgers University.
References
  1. Islam MM, Li Y, Luo H, Xiang M, Cai L. Meis1 regulates Foxn4 expression during retinal progenitor cell differentiation. Biol Open. 2013 Sep 6;2(11):1125-36.

If you publish research with this product, please let us know so we can cite your paper.

 
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