Wang Sidney H, Nan Ruth, Accardo Maria C, Sentmanat Monica, Dimitri Patrizio, Elgin Sarah C R
Department of Biology, Washington University, St. Louis, Missouri, United States of America.
Dipartimento di Biologia e Biotecnologie "Charles Darwin" and Istituto Pasteur Fondazione Cenci-Bolognetti, Sapienza Università di Roma, Roma, Italy.
PLoS One. 2014 Jan 24;9(1):e86451. doi: 10.1371/journal.pone.0086451. eCollection 2014.
Heterochromatin assembly and its associated phenotype, position effect variegation (PEV), provide an informative system to study chromatin structure and genome packaging. In the fruit fly Drosophila melanogaster, the Y chromosome is entirely heterochromatic in all cell types except the male germline; as such, Y chromosome dosage is a potent modifier of PEV. However, neither Y heterochromatin composition, nor its assembly, has been carefully studied. Here, we report the mapping and characterization of eight reporter lines that show male-specific PEV. In all eight cases, the reporter insertion sites lie in the telomeric transposon array (HeT-A and TART-B2 homologous repeats) of the Y chromosome short arm (Ys). Investigations of the impact on the PEV phenotype of mutations in known heterochromatin proteins (i.e., modifiers of PEV) show that this Ys telomeric region is a unique heterochromatin domain: it displays sensitivity to mutations in HP1a, EGG and SU(VAR)3-9, but no sensitivity to Su(z)2 mutations. It appears that the endo-siRNA pathway plays a major targeting role for this domain. Interestingly, an ectopic copy of 1360 is sufficient to induce a piRNA targeting mechanism to further enhance silencing of a reporter cytologically localized to the Ys telomere. These results demonstrate the diversity of heterochromatin domains, and the corresponding variation in potential targeting mechanisms.
异染色质组装及其相关表型——位置效应斑驳(PEV),为研究染色质结构和基因组包装提供了一个信息丰富的系统。在果蝇黑腹果蝇中,除雄性生殖系外,Y染色体在所有细胞类型中均完全为异染色质;因此,Y染色体剂量是PEV的一个强大修饰因子。然而,Y异染色质的组成及其组装都尚未得到仔细研究。在这里,我们报告了八个显示雄性特异性PEV的报告系的定位和表征。在所有八个案例中,报告基因插入位点位于Y染色体短臂(Ys)的端粒转座子阵列(HeT-A和TART-B2同源重复序列)中。对已知异染色质蛋白(即PEV修饰因子)突变对PEV表型影响的研究表明,这个Ys端粒区域是一个独特的异染色质结构域:它对HP1a、EGG和SU(VAR)3-9的突变敏感,但对Su(z)2突变不敏感。似乎内源性小干扰RNA途径对这个结构域起主要靶向作用。有趣的是,1360的一个异位拷贝足以诱导一种piRNA靶向机制,以进一步增强对细胞学定位在Ys端粒的报告基因的沉默。这些结果证明了异染色质结构域的多样性以及潜在靶向机制的相应变化。