Homez, a homeobox leucine zipper gene specific to the vertebrate lineage

被引:15
作者
Bayarsaihan, D
Enkhmandakh, B
Makeyev, A
Greally, JM
Leckman, JF
Ruddle, FH
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06520 USA
[2] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Med Hematol, Bronx, NY 10461 USA
[4] Yale Univ, Sch Med, Ctr Child Study, New Haven, CT 06520 USA
关键词
D O I
10.1073/pnas.1834010100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This work describes a vertebrate homeobox gene, designated Homez (homeodomain leucine zipper-encoding gene), that encodes a protein with an unusual structural organization. There are several regions within Homez, including three atypical homeodomains, two leucine zipper-like motifs, and an acidic domain. The gene is ubiquitously expressed in human and murine tissues, although the expression pattern is more restricted during mouse development. Genomic analysis revealed that human and mouse genes are located at 14q11.2 and 14C, respectively, and are composed of two exons. The zebrafish and pufferfish homologs share high similarity to mammalian sequences, particularly within the homeodomain sequences. Based on homology of homeodomains and on the similarity in overall protein structure, we deliniate Hornez and members of ZHX family of zinc finger homeodomain factors as a subset within the superfamily of homeobox-containing proteins. The type and composition of homeodomains in the Hornez subfamily are vertebrate-specific. Phylogenetic analysis indicates that Homez lineage was separated from related genes >400 million years ago before separation of ray- and lobe-finned fishes. We apply a duplication-degeneration-complementation model to explain how this family of genes has evolved.
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页码:10358 / 10363
页数:6
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