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Cloning and expression of Xenopus Lrp5 and Lrp6 genes
Journal article   Open access   Peer reviewed

Cloning and expression of Xenopus Lrp5 and Lrp6 genes

Douglas W Houston and Chris Wylie
Mechanisms of development, Vol.117(1), pp.337-342
2002
DOI: 10.1016/S0925-4773(02)00205-8
PMID: 12204281
url
https://doi.org/10.1016/S0925-4773(02)00205-8View
Published (Version of record) Open Access

Abstract

LRP5 and LRP6 comprise a subfamily of lipoprotein-receptor related proteins that function as co-receptors for Wnt proteins. Mutation of human LRP5 is responsible for osteoporosis-pseudoglioma syndrome and disruption of Lrp6 in mice causes similar effects to mutation of several different Wnt genes. We have cloned Xenopus homologues of Lrp5 and Lrp6 ( Xlrp5, Xlrp6) and examined their expression during embryogenesis. Both genes are expressed maternally and ubiquitously through early development. At later stages, Xlrp5 is found in the eye, forebrain, hindbrain, branchial arches and the tip of the tail bud. Xlrp6 is expressed throughout the central nervous system, branchial arches, in the eye and otic vesicle. Both genes are also expressed at the intersomitic boundary. These results suggest roles for Wnt signaling via LRP proteins in these tissues.
Xenopus Arrow Co-receptor Lipoprotein receptor-related protein Lrp6 Osteoporosis-pseudoglioma Wnt Lrp5

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