Academic Endocrine Unit, Nuffield Department of Clinical Medicine, Oxford Centre for Diabetes, Endocrinology and Metabolism (OCDEM), University of Oxford, Oxford, OX3 7LJ, UK.
Horm Cancer. 2013 Jun;4(3):123-39. doi: 10.1007/s12672-013-0138-x. Epub 2013 Feb 22.
Somatic and germline mutations in the dual zinc-finger transcription factor GATA3 are associated with breast cancers expressing the estrogen receptor (ER) and the autosomal dominant hypoparathyroidism-deafness-renal dysplasia syndrome, respectively. To elucidate the role of GATA3 in breast tumorigenesis, we investigated 40 breast cancers that expressed ER, for GATA3 mutations. Six different heterozygous GATA3 somatic mutations were identified in eight tumors, and these consisted of: a frameshifting deletion/insertion (944_945delGGinsAGC), an in-frame deletion of a key arginine residue (991_993delAGG), a seven-nucleotide frameshifting insertion (991_992insTGGAGGA), a frameshifting deletion (1196_1197delGA), and two frameshifting single nucleotide insertions (1224_1225insG found in three tumors and 1224_1225insA). Five of the eight mutations occurred in tumors that retained GATA3 immunostaining, indicating that absence of GATA3 immunostaining is an unreliable predictor of the presence of GATA3 mutations. Luciferase reporter assays, electrophoretic mobility shift assays, immunofluorescence, invasion and proliferation assays demonstrated that the GATA3 mutations resulted in loss (or reduction) of DNA binding, decrease in transactivational activity, and alterations in invasiveness but not proliferation. The 991_992insTGGAGGA (Arg330 frameshift) mutation led to a loss of nuclear localization, yet the 991_993delAGG (Arg330deletion) retained nuclear localization. Investigation of the putative nuclear localization signal (NLS) sites showed that the NLS of GATA3 does not conform to either a classical mono- or bi-partite signal, but contains multiple cooperative NLS elements residing around the N-terminal zinc-finger which comprises residues 264-288. Thus, approximately 20 % ER-positive breast cancers have somatic GATA3 mutations that lead to a loss of GATA3 transactivation activity and altered cell invasiveness.
双锌指转录因子 GATA3 的体细胞和种系突变分别与表达雌激素受体 (ER) 的乳腺癌和常染色体显性低钙血症-耳聋-肾发育不良综合征相关。为了阐明 GATA3 在乳腺癌发生中的作用,我们研究了 40 例表达 ER 的乳腺癌,以确定 GATA3 突变情况。在 8 个肿瘤中发现了 6 种不同的杂合 GATA3 体细胞突变,包括:一个框移缺失/插入 (944_945delGGinsAGC)、一个关键精氨酸残基的框移缺失 (991_993delAGG)、一个七核苷酸框移插入 (991_992insTGGAGGA)、一个框移缺失 (1196_1197delGA) 和两个框移单核苷酸插入 (1224_1225insG,在 3 个肿瘤中发现,1224_1225insA)。这 8 个突变中有 5 个发生在保留 GATA3 免疫染色的肿瘤中,这表明 GATA3 免疫染色缺失并不是 GATA3 突变存在的可靠预测指标。荧光素酶报告基因分析、电泳迁移率变动分析、免疫荧光、侵袭和增殖分析表明,GATA3 突变导致 DNA 结合丧失(或减少)、转录激活活性降低以及侵袭性改变,但不影响增殖。991_992insTGGAGGA (Arg330 框移) 突变导致核定位丧失,但 991_993delAGG (Arg330 缺失) 保留核定位。对假定核定位信号 (NLS) 位点的研究表明,GATA3 的 NLS 不符合经典的单或双部分信号,而是包含多个位于包含残基 264-288 的 N 端锌指周围的协同 NLS 元件。因此,大约 20%的 ER 阳性乳腺癌存在导致 GATA3 转录激活活性丧失和细胞侵袭性改变的体细胞 GATA3 突变。