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[Cancer Research 48, 645-649, February 1, 1988]
© 1988 American Association for Cancer Research

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Expression of Two Different Endogenous Galactoside-binding Lectins Sharing Sequence Homology1

Avraham Raz2, Pnina Carmi and Galit Pazerini

Department of Cell Biology, The Weizmann Institute of Science, P.O. Box 26, Rehovot, Israel

The endogenous ß-D-galactoside-binding lectins of UV-2237-IP3 fibrosarcoma cells consist of two polypeptides with molecular weights of 14,500 (L-14.5) and 34,000 (L-34). Recently we constructed complementary DNA (cDNA) libraries from these cells in the expression vector {lambda}gt11 and isolated and characterized cDNA clones encoding the two lectin species (A. Raz et al., Exp. Cell Res., 173: 109, 1987). We report here on the similarity in structure and gene number in genomic DNA of the fibrosarcoma cells and syngeneic normal mouse lung DNA. The expression of mRNAs hybridizing to these cDNAs was evaluated in three pairs of normal versus their transformed cell variants. Messenger RNA corresponding to the Mr 34,000 lectin was present more abundantly in the transformed cells than in their normal counterparts, while no difference was detected between the cell pairs with respect to mRNA levels corresponding to the Mr 14,500 lectin. We have established the nucleotide sequences of the two cDNA clones. The deduced amino acid sequence of L-14.5 lectin cDNA clone (L-3) is significantly homologous to the sequence of six other L-14 vertebrate galactoside binding lectins. The sequence of the Mr 34,000 lectin cDNA clone (M5) revealed that it shares a stretch of 39 amino acids with all of the L-14 galactoside binding lectins, irrespective of origin of the species, suggesting both that they are all derived from a common ancestral gene, and that this domain is necessary for similar sugar binding properties.

1 This investigation was supported by USPHS Grant CA46120, awarded by the National Cancer Institute, Department of Health and Human Services, to A. R.

2 Incumbent of the Sophie M. T. and Richard S. Richards Career Development Chair in Cancer Research. Present address, Cancer Metastasis Program, Michigan Cancer Foundation, Meyer L. Prentis Cancer Center, 110 E. Warren Avenue, Detroit, Michigan 48201.

Received 8/ 3/87. Revised 10/26/87. Accepted 10/29/87.




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HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
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Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1988 by the American Association for Cancer Research.