Abstract

The full-length mouse Indian hedgehog (Ihh) cDNA was cloned from an embryonic 17.5-day kidney library and was used to study the post-translational processing of the peptide and temporal and spatial expression of the transcript. Sequence analysis predicted two putative translation initiation sites. Ihh translation was initiated at both initiation sites when expressed in an in vitro transcription/translation system. Expression of an Ihh mutant demonstrated that the internal translation initiation site was sufficient to produce the mature forms of Ihh. Ihh post-translational processing proceeded in a fashion similar to Sonic and Drosophila hedgehog; the unprocessed form underwent signal peptide cleavage as well as internal proteolytic processing to form a 19-kDa amino-terminal peptide and a 26-kDa carboxyl-terminal peptide. This processing required His313 present in a conserved serine protease motif. Ihh transcript was detected by in situ RNA hybridization as early as 10 days postcoitum (dpc) in developing gut, as early as 14.5 dpc in the cartilage primordium, and in the developing urogenital sinus. In semiquantitative reverse transcription-polymerase chain reaction experiments, Indian hedgehog transcript was first detected in the mouse metanephros at 14.5 dpc; transcript abundance increased with gestational age, becoming maximal in adulthood. In adult kidney, Ihh transcript was detected only in the proximal convoluted tubule and proximal straight tubule.

Highlights

  • Mouse Indian hedgehog (Ihh)1 is a member of a multigene family that includes Hedgehog (Drosophila) and its vertebrate homologue, Sonic hedgehog [1, 2]

  • Isolation and Molecular Cloning of Full-length Mouse Ihh cDNA—The complete Ihh coding region was assembled from a set of six overlapping cDNA clones isolated from an embryonic 17.5 dpc kidney cDNA library

  • The 1008 bp overlapping the published partial cDNA sequence of Ihh contained a single base change resulting in an arginine to tryptophan substitution at amino acid 171 and a two-base substitution altering amino acid 421 from a serine to a tryptophan [2]

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Summary

Introduction

Mouse Indian hedgehog (Ihh) is a member of a multigene family that includes Hedgehog (Drosophila) and its vertebrate homologue, Sonic hedgehog [1, 2]. Shh affects the dorsoventral patterning of the mouse neural tube and somites leading to the induction of floor plate cells, motor neurons, and sclerotome [12,13,14,15]. Both Hh and Shh undergo autoproteolytic cleavage to generate a functional amino-terminal peptide, with inducing activity, and a carboxyl-terminal peptide that can tether the precursor protein to the cell membrane (14 –20). For Ihh, partial cDNA sequences are available for human and mouse with expression reported in the embryonic lung of human, the developing gut and cartilage of chick, and the adult kidney in both mouse and human [2, 21,22,23]. The Ihh transcript localized to the proximal convoluted and proximal straight tubule in the adult kidney

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