Blümer Nicole, Schreiter Kay, Hempel Leonie, Santel Ansgar, Hollmann Martin, Schäfer Mireille A, Renkawitz-Pohl Renate
FB Biologie, Entwicklungsbiologie, Philipps-Universität Marburg, Karl-von-Frisch-Strasse, 35043 Marburg, Germany.
Mech Dev. 2002 Jan;110(1-2):97-112. doi: 10.1016/s0925-4773(01)00577-9.
The Drosophila don juan (dj) gene encodes a basic protein that is expressed solely in the male germline and shows structural similarities to the linker histone H1. Don Juan is located in two different subcellular structures: in the nucleus during the phase of chromatin condensation and later in the mitochondrial derivatives starting with spermatid individualization. The don juan gene is transcribed in primary spermatocytes under the control of 23 bp upstream in combination with downstream sequences. During meiotic stages and in early spermatid stages don juan mRNA is translationally repressed for several days. Analysis of male sterile mutants which fail to undergo meiosis shows that release of dj mRNA from translational repression is independent of meiosis. In gel retardation assays 60 nucleotides at the end of the dj leader form four major complexes with proteins that were extracted from testes but not with protein extracts from ovaries. Transformation studies prove that in vivo 35 bp within that region of the dj mRNA is essential to confer translational repression. UV cross-linking studies show that a 62 kDa protein specifically binds to the same region within the 5' untranslated region. The dj translational repression element, TRE, is distinct from the translational control element, TCE, described earlier for all members of the Mst(3)CGP gene family. Moreover, expression studies in several male sterile mutants reveal that don juan mRNA is translated in earlier developmental stages during sperm morphogenesis than the Mst(3)CGP mRNAs. This proves that translational activation of dormant mRNAs in spermatogenesis occurs at different time-points which are characteristic for each gene, an essential feature for coordinated sperm morphogenesis.
果蝇的唐璜(dj)基因编码一种碱性蛋白,该蛋白仅在雄性生殖系中表达,并且与连接组蛋白H1具有结构相似性。唐璜定位于两种不同的亚细胞结构中:在染色质浓缩阶段位于细胞核中,随后在精子个体化开始时位于线粒体衍生物中。唐璜基因在初级精母细胞中,在23 bp上游序列与下游序列的共同控制下进行转录。在减数分裂阶段和早期精子细胞阶段,唐璜mRNA的翻译被抑制数天。对未能进行减数分裂的雄性不育突变体的分析表明,唐璜mRNA从翻译抑制中释放出来与减数分裂无关。在凝胶阻滞试验中,唐璜基因前导序列末端的60个核苷酸与从睾丸中提取的蛋白质形成四种主要复合物,但不与从卵巢中提取的蛋白质提取物形成复合物。转化研究证明,在体内,唐璜mRNA该区域内的35 bp对于赋予翻译抑制作用至关重要。紫外线交联研究表明,一种62 kDa的蛋白质特异性结合到5'非翻译区内的同一区域。唐璜翻译抑制元件(TRE)与先前针对Mst(3)CGP基因家族所有成员描述的翻译控制元件(TCE)不同。此外,在几个雄性不育突变体中的表达研究表明,在精子形态发生的早期发育阶段,唐璜mRNA比Mst(3)CGP mRNA更早被翻译。这证明了精子发生过程中休眠mRNA的翻译激活发生在每个基因特有的不同时间点,这是协调精子形态发生的一个基本特征。