Literature DB >> 12427544

The BSP30 salivary proteins from cattle, LUNX/PLUNC and von Ebner's minor salivary gland protein are members of the PSP/LBP superfamily of proteins.

Thomas T Wheeler1, Brendan J Haigh, Judith Y McCracken, Richard J Wilkins, Chris A Morris, Murray R Grigor.   

Abstract

Saliva influences rumen function in cattle, yet the biochemical role for most of the bovine salivary proteins (BSPs) has yet to be established. Two cDNAs (BSP30a and BSP30b) from bovine parotid salivary gland were cloned and sequenced, each coding for alternate forms of a prominent protein in bovine saliva. The BSP30 cDNAs share 96% sequence identity with each other at the DNA level and 83% at the amino acid level, and appear to arise from separate genes. The predicted BSP30a and BSP30b proteins share 26-36% amino acid identity with parotid secretory protein (PSP) from mouse, rat and human. BSP30 and PSP are in turn more distantly related to a wider group of proteins that includes lung-specific X protein, also known as palate, lung, and nasal epithelium clone (LUNX/PLUNC), von Ebner's minor salivary gland protein (VEMSGP), bactericidal permeability increasing protein (BPI), lipopolysaccharide binding protein (LBP), cholesteryl ester transfer protein (CETP), and the putative olfactory ligand-binding proteins RYA3 and RY2G5. Bovine cDNAs encoding homologs of LUNX/PLUNC and VEMSGP were isolated and sequenced. Northern blot analysis showed that LUNX/PLUNC, BSP30 and VEMSGP are expressed in bovine salivary tissue and airways, and that they have non-identical patterns of expression in these tissues. The expression of both BSP30a and BSP30b is restricted to salivary tissue, but within this tissue they have distinct patterns of expression. The proximity of the human genes coding for the PSP/LBP superfamily on HSA20q11.2, their similar amino acid sequence, and common exon segmentation strongly suggest that these genes evolved from a common ancestral gene. Furthermore, they imply that the BSP30a and BSP30b proteins may have a function in common with other members of this gene family.

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Year:  2002        PMID: 12427544     DOI: 10.1016/s0167-4781(02)00508-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  13 in total

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Review 2.  Collectins and cationic antimicrobial peptides of the respiratory epithelia.

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Journal:  J Infect Dis       Date:  2011-09-07       Impact factor: 5.226

4.  Human LPLUNC1 is a secreted product of goblet cells and minor glands of the respiratory and upper aerodigestive tracts.

Authors:  Colin D Bingle; Kirsty Wilson; Hayley Lunn; Frances A Barnes; Alec S High; William A Wallace; Doris Rassl; Michael A Campos; Manuel Ribeiro; Lynne Bingle
Journal:  Histochem Cell Biol       Date:  2010-03-18       Impact factor: 4.304

5.  Characterisation and expression of SPLUNC2, the human orthologue of rodent parotid secretory protein.

Authors:  Lynne Bingle; Frances A Barnes; Hayley Lunn; Maslinda Musa; Steve Webster; C W Ian Douglas; Simon S Cross; Alec S High; Colin D Bingle
Journal:  Histochem Cell Biol       Date:  2009-06-05       Impact factor: 4.304

6.  Phylogenetic and evolutionary analysis of the PLUNC gene family.

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Journal:  Protein Sci       Date:  2004-02       Impact factor: 6.725

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Authors:  Emanuele Cotroneo; Gordon B Proctor; Guy H Carpenter
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9.  Expansion of the Bactericidal/Permeability Increasing-like (BPI-like) protein locus in cattle.

Authors:  Thomas T Wheeler; Kylie A Hood; Nauman J Maqbool; John C McEwan; Colin D Bingle; Shaying Zhao
Journal:  BMC Genomics       Date:  2007-03-15       Impact factor: 3.969

10.  Differential epithelial expression of the putative innate immune molecule SPLUNC1 in cystic fibrosis.

Authors:  Lynne Bingle; Frances A Barnes; Simon S Cross; Doris Rassl; William A Wallace; Michael A Campos; Colin D Bingle
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