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果蝇中由标记的P因子插入诱变诱导的多同源异型额外梳状表型的显性修饰因子。

Dominant modifiers of the polyhomeotic extra-sex-combs phenotype induced by marked P element insertional mutagenesis in Drosophila.

作者信息

Fauvarque M O, Laurenti P, Boivin A, Bloyer S, Griffin-Shea R, Bourbon H M, Dura J M

机构信息

Institut de Génétique Humaine, CNRS/UPR 1142, 141 rue de la Cardonille, 34396 Montpellier, France.

出版信息

Genet Res. 2001 Oct;78(2):137-48. doi: 10.1017/s0016672301005274.

Abstract

Members of the Polycomb group (Pc-G) and trithorax group (trx-G) of genes, as well as the enhancers of trx-G and Pc-G (ETP), function together to maintain segment identity during Drosophila development. In order to obtain new marked P mutations in these genes, we screened for dominant modifiers of the extra-sex-combs phenotype displayed by males mutant for the polyhomeotic (ph) gene, a member of the Pc-G group. Five P(lacW) insertions in four different genes were found to stably suppress ph: two are allelic to trithorax, one is the first allele specific to the Minute(2)21C gene, and the remaining two define new trx-G genes, toutatis (tou) in 48A and taranis (tara) in 89B10-13. tou is predicted to encode a 3109 amino acid sequence protein (TOU), which contains a TAM DNA-binding domain, a WAKZ motif, two PHD zinc fingers and a C-terminal bromodomain, and as such is likely to be involved in regulation of chromatin structure as a subunit of a novel chromatin remodelling complex. In a previous study, we found that insertion of a P(ph) transposable element containing ph regulatory sequences creates a high frequency of mutations modifying ph homeotic phenotypes. One such insertion enhanced the ph phenotype and we show that it is a new allele of UbcD1/eff, a gene encoding a ubiquitin-conjugating enzyme that is involved in telomere association and potentially in chromatin remodelling.

摘要

多梳基因家族(Pc-G)和三胸节基因家族(trx-G)的成员,以及trx-G和Pc-G的增强子(ETP),在果蝇发育过程中共同作用以维持体节特征。为了在这些基因中获得新的标记P突变,我们筛选了多梳基因家族成员多体节同源基因(ph)突变的雄性果蝇所表现出的超性梳表型的显性修饰因子。在四个不同基因中发现了五个P(lacW)插入稳定抑制ph:两个与三胸节基因等位,一个是微小(2)21C基因特有的第一个等位基因,其余两个定义了新的trx-G基因,位于48A的toutatis(tou)和位于89B10 - 13的taranis(tara)。预测tou编码一个3109个氨基酸序列的蛋白质(TOU),它包含一个TAM DNA结合结构域、一个WAKZ基序、两个PHD锌指和一个C端溴结构域,因此可能作为一种新型染色质重塑复合物的亚基参与染色质结构的调控。在先前的一项研究中,我们发现插入含有ph调控序列的P(ph)转座元件会产生高频率的修饰ph同源异型表型的突变。其中一个这样的插入增强了ph表型,我们表明它是UbcD1/eff的一个新等位基因,UbcD1/eff是一个编码泛素结合酶的基因,该酶参与端粒关联并可能参与染色质重塑。

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