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棕色棉(Gossypium hirsutum L.)透明种皮 12 同源基因的分子克隆、表达分析及亚细胞定位

Molecular cloning, expression analysis and subcellular localization of a Transparent Testa 12 ortholog in brown cotton (Gossypium hirsutum L.).

机构信息

School of Life Sciences, Anhui Agricultural University, Hefei 230036, China.

Institute of Agricultural Economy and Information, Anhui Academy of Agricultural Sciences, Hefei 230031, China.

出版信息

Gene. 2016 Feb 1;576(2 Pt 2):763-9. doi: 10.1016/j.gene.2015.11.002. Epub 2015 Nov 11.

DOI:10.1016/j.gene.2015.11.002
PMID:26548815
Abstract

Transparent Testa 12 (TT12) is a kind of transmembrane transporter of proanthocyanidins (PAs), which belongs to a membrane-localized multidrug and toxin efflux (MATE) family, but the molecular basis of PAs transport is still poorly understood. Here, we cloned a full-length TT12 cDNA from the fiber of brown cotton (Gossypium hirsutum), named GhTT12 (GenBank accession No. KF240564), which comprised 1733 bp with an open reading frame (ORF) of 1503 bp and encoded a putative protein containing 500 amino acid residues with a typical MATE conserved domain. The GhTT12 gene had 96.8% similarity to AA genome in Gossypium arboretum. Quantitative RT-PCR analysis denoted that the relative expression of GhTT12 in brown cotton was 1-5 folds higher than that in white cotton. The mRNA level was the highest at 5 days post anthesis (DPA) and reduced gradually during the fiber development. Expressing GhTT12-fused green fluorescent protein (GFP) in Nicotiana tabacum showed that GhTT12-GFP was localized in the vacuole membrane. The content of PAs increased firstly and decreased afterwards, and reached the maximum at 15 DPA in brown cotton. But for white cotton, the content of PAs remained at a low level during the fiber development. We speculate that GhTT12 may participate in the transportation of PAs from the cytoplasmic matrix to the vacuole. Taken together, our data revealed that GhTT12 was functional as a PAs transmembrane transporter.

摘要

透明种皮 12 号(TT12)是原花青素(PAs)的一种跨膜转运蛋白,属于膜定位多药和毒素外排(MATE)家族,但 PAs 转运的分子基础仍知之甚少。在这里,我们从棕色棉花(Gossypium hirsutum)的纤维中克隆了一个全长 TT12 cDNA,命名为 GhTT12(GenBank 登录号 KF240564),它由 1733bp 组成,开放阅读框(ORF)为 1503bp,编码一个含有 500 个氨基酸残基的假定蛋白,具有典型的 MATE 保守结构域。GhTT12 基因与 Gossypium arboretum 的 AA 基因组有 96.8%的相似性。定量 RT-PCR 分析表明,棕色棉花中 GhTT12 的相对表达量比白色棉花高 1-5 倍。在开花后 5 天(DPA)mRNA 水平最高,随后在纤维发育过程中逐渐降低。在烟草中表达 GhTT12 融合绿色荧光蛋白(GFP)表明 GhTT12-GFP 定位于液泡膜。棕色棉花中 PAs 的含量先增加后减少,在 15 DPA 时达到最大值。但对于白色棉花,PAs 的含量在纤维发育过程中一直保持在较低水平。我们推测 GhTT12 可能参与了 PAs 从细胞质基质到液泡的转运。总之,我们的数据表明 GhTT12 是一种功能性的 PAs 跨膜转运蛋白。

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