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Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16

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Summary

Twenty-three independent man-hamster (CH/HGPRT-) hybrids were analysed for human acid lipases and for some other human enzyme markers (PP, GOT 1, PGP) and chromosomes. Eighteen independent man-mouse (LA/HGPRT-TK) hybrids were analysed for human acid lipases, human enzyme marker PGP and human chromosomes.

Three fibroblasts from unrelated patients with WD (Wolman's disease), one fibroblast from a heterozygote for WD, and 15 normal fibroblasts were analysed for acid lipases.

The following results were obtained:

  1. 1)

    A positive correlation was observed between acid lipase A and Chr. 10, and between acid lipase B and Chr. 16. In fact, among 23 independent man-hamster hybrids, 6 were Chr. 10+PP+GOT 1+LIP A+ and 17 were Chr. 10-PP-GOT 1-LIP A-, and among 41 independent man-rodent hybrids 23 were Chr. 16+ PGP+LIP B+ and 18 were Chr. 16-PGP-LIP B-. Except for Chr. 10, the other autosomes were observed in hybrids LIP A, and except for Chr. 16, the other autosomes were observed in hybrids LIP B-.

    These results indicate that the gene for lipase A is on Chr. 10 and the gene for lipase B is on Chr. 16.

  2. 2)

    The acid lipase A is deficient in WD fibroblasts. Therefore the mutation responsible for WD is on Chr. 10. The B, C and at least three additional lipases were observed in WD fibroblasts and in WD heterozygote fibroblasts at pH 4.0 and with 4-methylumbelliferyl oleate as substrate. The relationship between these different acid lipases are obscure. In the normal fibroblasts from healthy control subjects a considerable variation in acid lipase A activity was observed. In some normal fibroblasts from healthy control subjects, in which the lipase A is reduced, we observed the same acid lipase zymogram pattern as in WD heterozygote fibroblasts.

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Van Cong, N., Weil, D., Hors-Cayla, M.C. et al. Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16. Hum Genet 55, 375–381 (1980). https://doi.org/10.1007/BF00290221

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