Identification of SCML2, a second human gene homologous to the Drosophila Sex comb on midleg (Scm): A new gene cluster on Xp22

Eugenio Montini, Georg Buchner, Cosma Spalluto, Grazia Andolfi, Antonio Caruso, Johan T. Den Dunnen, Dorothy Trump, Mariano Rocchi, Andrea Ballabio, Brunella Franco

Research output: Contribution to journalArticlepeer-review

Abstract

We have identified a novel gene with homologies to the Drosophila Sex comb on midleg (Scm) gene from the short arm of the X chromosome. Scm is a member of the Polycomb group (PcG) genes, which encode transcriptional repressors essential for appropriate development in the fly and in mammals. The newly identified transcript named SCML2 (sex comb on midleg like-2, HGMW- approved symbol) is ubiquitously expressed and encodes a protein of 700 amino acids. SCML2 maps very close to the recently identified SCML1, revealing the presence of a new gene cluster in Xp22. The homology and map location identify SCML2 as a candidate gene for Xp22-linked developmental disorders, including the oral-facial-digital type I (OFDI) syndrome. A study of the SCML1-SCML2 cluster in primates indicates that the two genes are localized to the same region in Old World monkeys, New World monkeys, and promisians, suggesting that the duplication event leading to the formation of the SCML cluster on Xp22 occurred before primate divergence.

Original languageEnglish
Pages (from-to)65-72
Number of pages8
JournalGenomics
Volume58
Issue number1
DOIs
Publication statusPublished - May 15 1999

ASJC Scopus subject areas

  • Genetics

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