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两种锌转运蛋白SLC30A5和SLC30A6的表达改变是乳腺向乳汁中分泌锌减少这一病症的基础。

Altered expression of two zinc transporters, SLC30A5 and SLC30A6, underlies a mammary gland disorder of reduced zinc secretion into milk.

作者信息

Kumar Loveleen, Michalczyk Agnes, McKay Jill, Ford Dianne, Kambe Taiho, Hudek Lee, Varigios George, Taylor Philip E, Ackland M Leigh

机构信息

Centre for Cellular and Molecular Biology, School of Life and Environmental Sciences, Deakin University, 221 Burwood Highway, Burwood, VIC, 3125, Australia.

出版信息

Genes Nutr. 2015 Sep;10(5):487. doi: 10.1007/s12263-015-0487-x. Epub 2015 Aug 29.

Abstract

Two cases of zinc deficiency in breastfed neonates were investigated where zinc levels in the mothers' milk were reduced by more than 75 % compared to normal. The objective of this study was to find the molecular basis of the maternal zinc deficiency condition. Significant reductions in mRNA expression and protein levels of the zinc transporters SLC30A5 and SLC30A6 were found in maternal tissue, suggesting a causal link to the zinc-deficient milk. Novel splice variants of the SLC30A6 transcript were detected. No modifications were found in coding regions, or in transcription binding sites of promoter regions or in 5' and 3' untranslated regions of both transporters in lymphoblasts and fibroblasts isolated from both mothers. Altered DNA methylation in SLC30A5 at two CpG sites was detected and may account for the reduced levels of SLC30A5 mRNA and protein in lymphoblasts. Reduced SLC30A6 mRNA and protein levels in lymphoblasts may be secondary to reduced SLC30A5 expression, as they function as a heterodimer in zinc transport. In conclusion, two cases of zinc deficiency are linked to low levels of the SLC30A5 and SLC30A6 zinc transporters. These two zinc transporters have not been previously associated with zinc deficiency in milk.

摘要

对两例母乳喂养新生儿锌缺乏病例进行了调查,其母乳中的锌水平相较于正常情况降低了75%以上。本研究的目的是找出母体锌缺乏状况的分子基础。在母体组织中发现锌转运蛋白SLC30A5和SLC30A6的mRNA表达及蛋白水平显著降低,提示其与缺锌母乳存在因果关系。检测到了SLC30A6转录本的新型剪接变体。在从两位母亲分离出的淋巴母细胞和成纤维细胞中,这两种转运蛋白的编码区、启动子区转录结合位点以及5'和3'非翻译区均未发现修饰。检测到SLC30A5两个CpG位点的DNA甲基化改变,这可能是淋巴母细胞中SLC30A5 mRNA和蛋白水平降低的原因。淋巴母细胞中SLC30A6 mRNA和蛋白水平降低可能继发于SLC30A5表达降低,因为它们在锌转运中作为异二聚体发挥作用。总之,两例锌缺乏病例与SLC30A5和SLC30A6锌转运蛋白水平低有关。此前这两种锌转运蛋白与母乳中的锌缺乏并无关联。

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