Cléard F, Matsarskaia M, Spierer P
Department of Zoology and Animal Biology, University of Geneva, Chêne-Bougeries, Switzerland.
Nucleic Acids Res. 1995 Mar 11;23(5):796-802. doi: 10.1093/nar/23.5.796.
An increase in the number of copies of the Drosophila locus Suvar(3)7 enhances position-effect variegation, i.e. the inactivation in some cells of genes brought close to heterochromatin by a chromosomal rearrangement. The locus produces two transcripts of 5047 and 4203 nt that differ solely by the length of their 3' untranslated region. That these transcripts encode the modifier of variegation Suvar(3)7 is demonstrated by genetic transformation with the corresponding cDNAs. The deduced protein is 1169 amino acids long and contains seven widely spaced zinc fingers. These fingers are each preceded at 11-16 amino acids before the N-terminal cysteine by a tryptophan-containing motif. The transcripts are maternally transmitted, but are also found throughout development. The ubiquitous distribution of transcripts in embryos and the different sequence motifs support our speculation that the locus encodes a chromosomal protein implicated in heterochromatin-mediated DNA silencing.
果蝇位点Suvar(3)7的拷贝数增加会增强位置效应斑驳,即通过染色体重排靠近异染色质的基因在某些细胞中失活。该位点产生两种长度分别为5047和4203 nt的转录本,它们仅在3'非翻译区的长度上有所不同。通过用相应的cDNA进行遗传转化证明,这些转录本编码斑驳修饰因子Suvar(3)7。推导的蛋白质长1169个氨基酸,包含七个间隔很宽的锌指。在这些锌指的N端半胱氨酸之前的11 - 16个氨基酸处,每个锌指之前都有一个含色氨酸的基序。这些转录本是母系遗传的,但在整个发育过程中也能发现。转录本在胚胎中的普遍分布以及不同的序列基序支持了我们的推测,即该位点编码一种参与异染色质介导的DNA沉默的染色体蛋白。