Identification of galectin-4 isoforms in porcine small intestine

被引:8
作者
Wooters, MA [1 ]
Ropp, SL [1 ]
Erickson, AK [1 ]
机构
[1] S Dakota State Univ, Dept Vet Sci, Brookings, SD 57007 USA
关键词
galectin; intestine; porcine; isofoms; alternative splicing;
D O I
10.1016/j.biochi.2004.12.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lactose-binding proteins with molecular masses of 14-, 17-, 18, 28-, and 34-kDa were identified in extracts front porcine small intestinal mucosa. Amino acid sequence analysis of peptides generated by CNBr cleavage of the 34-kDa protein, the most abundant of these proteins, identified this protein as porcine galectin-4. To determine if it porcine homolog of murine galectin-6 is expressed in small intestine, primers for a reverse transcriptase-polymerase chain reaction (RT-PCR) were developed that amplified across the linker region of galactin-4, which is the region that differs between murine galectins-4 and -6. Using these primers, this RT-PCR approach identified two galectin-4 isoforms that differed in the length of their linker region. The larger isoform, galectin-4. 1, is nine amino acids longer in its linker region than the smaller isoform galectin-4.2. Based on nucleotide sequence similarities, the two isoforms are like splice variants of galectin-4 pre-mRNA and not products of separate genes like murine galectins-4 and -6. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:143 / 149
页数:7
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