ZIP13: A Study of Drosophila Offers an Alternative Explanation for the Corresponding Human Disease.

ZIP13: A Study of Drosophila Offers an Alternative Explanation for the Corresponding Human Disease.
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ZIP13:果蝇研究为相应的人类疾病提供了另一种解释

DOI:
10.3389/fgene.2017.00234
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发表时间:
2017
影响因子:
3.7
通讯作者:
Zhou B
Zhou B
中科院分区:
生物学3区
文献类型:
--
作者:
Xiao G;Zhou B

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The fruit fly Drosophila melanogaster has become an important model organism to investigate metal homeostasis and human diseases. Previously we identified dZIP13 (CG7816), a member of the ZIP transporter family (SLC39A) and presumably a zinc importer, is in fact physiologically primarily responsible to move iron from the cytosol into the secretory compartments in the fly. This review will discuss the implication of this finding for the etiology of Spondylocheirodysplasia-Ehlers-Danlos Syndrome (SCD–EDS), a human disease defective in ZIP13. We propose an entirely different model in that lack of iron in the secretory compartment may underlie SCD-EDS. Altogether three different working models are discussed, supported by relevant findings made in different studies, with uncertainties, and questions remained to be solved. We speculate that the distinct ZIP13 sequence features, different from those of all other ZIP family members, may confer it special transport properties.
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