Currie P D, Sullivan D T
Department of Biology, Syracuse University, New York 13244-1270.
Genetics. 1994 Oct;138(2):352-63.
We report here the isolation and characterization of genes from Drosophila that encode the glycolytic enzyme phosphoglyceromutase (PGLYM). Two genomic regions have been isolated that have potential to encode PGLYM. Their cytogenetic localizations have been determined by in situ hybridization to salivary gland chromosomes. One gene, Pglym78, is found at 78A/B and the other, Pglym87, at 87B4,5 of the Drosophila polytene map. Pglym78 transcription follows a developmental pattern similar to other glycolytic genes in Drosophila, i.e., substantial maternal transcript deposited during oogenesis; a decline in abundance in the first half of embryogenesis; a subsequent increase in the second half of embryogenesis which continues throughout larval life; a decline in pupae and a second increase to a plateau in adults. This transcript has been mapped by cDNA and genomic sequence comparison, RNase protection, and primer extension. Using similar analyses transcripts of Pglym87 could not be detected. Pglym78 has two introns which interrupt the coding region, while the Pglym87 gene lacks introns. This and other features support a model of retrotransposition mediated gene duplication for the origin of Pglym87. The apparent absence of a complete, intact coding frame and transcript suggest that Pglym87 is a pseudogene. However, retention of reading frame and codon bias suggests that Pglym87 may retain coding function, or may have been inactivated recently, substantially after the time of duplication, or that the molecular evolution of Pglym87 is unusual. Similarities of the unusual molecular evolution of Pglym87 and other proposed pseudogenes are discussed.
我们在此报告从果蝇中分离和鉴定编码糖酵解酶磷酸甘油变位酶(PGLYM)的基因。已分离出两个有可能编码PGLYM的基因组区域。通过与唾液腺染色体的原位杂交确定了它们的细胞遗传学定位。一个基因Pglym78位于果蝇多线图谱的78A/B处,另一个基因Pglym87位于87B4,5处。Pglym78的转录遵循与果蝇中其他糖酵解基因相似的发育模式,即在卵子发生期间沉积大量母体转录本;在胚胎发育的前半段丰度下降;在胚胎发育的后半段随后增加,并在整个幼虫期持续;在蛹期下降,在成虫期再次增加至稳定水平。该转录本已通过cDNA和基因组序列比较、RNA酶保护和引物延伸进行了定位。使用类似分析未检测到Pglym87的转录本。Pglym78有两个内含子打断编码区,而Pglym87基因没有内含子。这一点以及其他特征支持了Pglym87起源于逆转座介导的基因复制的模型。明显缺乏完整的编码框架和转录本表明Pglym87是一个假基因。然而,阅读框的保留和密码子偏好表明Pglym87可能保留编码功能,或者可能在复制后相当长的时间内最近才失活,或者Pglym87的分子进化是不寻常的。讨论了Pglym87与其他提议的假基因的异常分子进化的相似性。