ArticleThe Journal of cell biology1994
The mouse ileal lipid-binding protein gene: a model for studying axial patterning during gut morphogenesis.
Article in The Journal of cell biology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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Who cites it
20 citing papers in PubMed, 91 citations in OpenAlex.
- Fatty acid binding proteins have the potential to channel dietary fatty acids into enterocyte nuclei.Journal of lipid research · 2016Article
- Doublecortin and CaM kinase-like-1 and leucine-rich-repeat-containing G-protein-coupled receptor mark quiescent and cycling intestinal stem cells, respectively.Stem cells (Dayton, Ohio) · 2009Article
- GATA4 mediates gene repression in the mature mouse small intestine through interactions with friend of GATA (FOG) cofactors.Developmental biology · 2008Article
- Systemic overexpression of growth hormone (GH) in transgenic FVB/N inbred mice: an optimized model for holistic studies of molecular mechanisms underlying GH-induced kidney pathology.Transgenic research · 2008Article
- Article
- Bile acid transporters in health and disease.Xenobiotica; the fate of foreign compounds in biological systems · 2008Review
- Does abnormal bile acid metabolism contribute to NEC?Seminars in perinatology · 2008Review
- Gata4 is essential for the maintenance of jejunal-ileal identities in the adult mouse small intestine.Molecular and cellular biology · 2006Article
- Bile acids induce ileal damage during experimental necrotizing enterocolitis.Gastroenterology · 2006Article
- c-Myc is required for the formation of intestinal crypts but dispensable for homeostasis of the adult intestinal epithelium.Molecular and cellular biology · 2005Article
- Altered epithelial cell lineage allocation and global expansion of the crypt epithelial stem cell population are associated with ileitis in SAMP1/YitFc mice.The American journal of pathology · 2005Article
- Regulation of the ileal bile acid-binding protein gene: an approach to determine its physiological function(s).Molecular and cellular biochemistry · 2002Review
- Article
- Creating and maintaining the gastrointestinal ecosystem: what we know and need to know from gnotobiology.Microbiology and molecular biology reviews : MMBR · 1998Review
- Article
- An intestine-specific homeobox gene regulates proliferation and differentiation.Molecular and cellular biology · 1996Article
- A 20-nucleotide element in the intestinal fatty acid binding protein gene modulates its cell lineage-specific, differentiation-dependent, and cephalocaudal patterns of expression in transgenic mice.Proceedings of the National Academy of Sciences of the United States of America · 1995Article
- In vivo analysis of cadherin function in the mouse intestinal epithelium: essential roles in adhesion, maintenance of differentiation, and regulation of programmed cell death.The Journal of cell biology · 1995Article
- Expression of a human alpha-1,3/4-fucosyltransferase in the pit cell lineage of FVB/N mouse stomach results in production of Leb-containing glycoconjugates: a potential transgenic mouse model for studying Helicobacter pylori infection.Proceedings of the National Academy of Sciences of the United States of America · 1995Article
- Ileal lipid-binding protein (Illbp) gene maps to mouse chromosome 11.Mammalian genome : official journal of the International Mammalian Genome Society · 1994Article
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
Abstract
Normal, chimeric-transgenic, and transgenic mice have been used to study the axial patterns of ileal lipid-binding protein gene (Ilbp) expression during and after completion of gut morphogenesis. Ilbp is initially activated in enterocytes in bidirectional wave that expands proximally in the ileum and distally to the colon during late gestation and the first postnatal week. This activation occurs at the same time that a wave of cytodifferentiation of the gut endoderm is completing its unidirectional journey from duodenum to colon. The subsequent contraction of Ilbp's expression domain, followed by its reexpansion from the distal to proximal ileum, coincides with a critical period in gut morphogenesis (postnatal days 7-28) when its proliferative units (crypts) form, establish their final stem cell hierarchy, and then multiply through fission. The wave of reactivation is characterized by changing patterns of Ilbp expression: (a) at the proximal most boundary of the wave, villi contain a mixed population of scattered ileal lipid-binding protein (ILBP)-positive and ILBP-negative enterocytes derived from the same monoclonal crypt; (b) somewhat more distally, villi contain vertical coherent stripes of wholly ILBP-positive enterocytes derived from monoclonal crypts and adjacent, wholly ILBP-negative stripes of enterocytes emanating from other monoclonal crypts; and (c) more distally, all the enterocytes on a villus support Ilbp expression. Functional mapping studies of Ilbp's promoter in transgenic mice indicate that nucleotides -145 to +48 contain cis-acting elements sufficient to produce an appropriately directed distal-to-proximal wave of Ilbp activation in the ileum, to maintain an appropriate axial distribution of monophenotypic wholly reporter-positive villi in the distal portion of the ileum, as well as striped and speckled villi in the proximal portion of its expression domain, and to correctly support reporter production in villus-associated ileal enterocytes. Nucleotides -417 to -146 of Ilbp contain a "temporal" suppressor that delays initial ileal activation of the gene until the second postnatal week. Nucleotides -913 to -418 contain a temporal suppressor that further delays initial activation of the gene until the third to fourth postnatal week, a spatial suppressor that prohibits gene expression in the proximal quarter of the ileum and in the proximal colon, and a cell lineage suppressor that prohibits expression in goblet cells during the first two postnatal weeks.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.