Zmym2 Alters Expression of Key Craniofacial Genes

IF 2.4 4区 生物学 Q2 DEVELOPMENTAL BIOLOGY
genesis Pub Date : 2025-05-30 DOI:10.1002/dvg.70018
Karyn Jourdeuil, Karen M. Neilson, Andre L. P. Tavares, Sally A. Moody
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引用次数: 0

Abstract

To identify novel Six1-interacting proteins, we previously screened the fly interactome for Sine oculis-binding partners whose orthologues are also expressed in Xenopus embryos. We identified a zinc-finger MYM-containing protein—Zmym2—based on its sequence similarity in a few domains also found in the Drosophila and vertebrate Sine oculis-binding proteins (Sobp). Because recent studies established Zmym2 as a transcriptional repressor that interacts with Six4 during renal development, herein we assessed whether it interacts with Six1, can modify Six1's transcriptional activity, and is involved in cranial neural crest or placode gene expression. Although during early development Zmym2 is expressed in many of the same tissues as Six1 and contains several domains also found in Sobp, we did not detect any interaction by co-immunoprecipitation and did not detect any effect on Six1 + Eya1 transcriptional activity in cultured cells. Nonetheless, increasing the level of Zmym2 in embryos resulted in broader expression domains of neural border, neural tube and neural crest genes, and smaller placode gene domains. These results suggest that although Zmym2 is unlikely to be a bone fide Six1 interacting protein, it appears to indirectly antagonize Six1 function during cranial placode development, promoting neural plate and neural crest gene expression.

Zmym2改变颅面关键基因的表达
为了鉴定新的six1相互作用蛋白,我们先前筛选了苍蝇相互作用组,以寻找在非洲爪蟾胚胎中也表达同源物的Sine眼结合伴侣。基于在果蝇和脊椎动物Sine - oculus -binding protein (Sobp)中发现的几个结构域序列相似性,我们鉴定了一个含锌指mym的蛋白- zmym2。由于最近的研究证实Zmym2是一个在肾脏发育过程中与Six4相互作用的转录抑制因子,因此我们在此评估了Zmym2是否与Six1相互作用,是否可以改变Six1的转录活性,是否参与颅神经嵴或位基基因的表达。虽然在早期发育过程中,Zmym2在许多与Six1相同的组织中表达,并且包含Sobp中也发现的几个结构域,但我们没有发现通过共免疫沉淀的任何相互作用,也没有发现在培养细胞中对Six1 + Eya1转录活性有任何影响。然而,增加胚胎中Zmym2的表达水平,导致神经边界、神经管和神经嵴基因的表达域变宽,而基板基因的表达域变小。这些结果表明,尽管Zmym2不太可能是一个骨性Six1相互作用蛋白,但它似乎在颅骨基板发育过程中间接拮抗Six1功能,促进神经板和神经嵴基因的表达。
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来源期刊
genesis
genesis 生物-发育生物学
CiteScore
3.60
自引率
0.00%
发文量
40
审稿时长
6-12 weeks
期刊介绍: As of January 2000, Developmental Genetics was renamed and relaunched as genesis: The Journal of Genetics and Development, with a new scope and Editorial Board. The journal focuses on work that addresses the genetics of development and the fundamental mechanisms of embryological processes in animals and plants. With increased awareness of the interplay between genetics and evolutionary change, particularly during developmental processes, we encourage submission of manuscripts from all ecological niches. The expanded numbers of genomes for which sequencing is being completed will facilitate genetic and genomic examination of developmental issues, even if the model system does not fit the “classical genetic” mold. Therefore, we encourage submission of manuscripts from all species. Other areas of particular interest include: 1) the roles of epigenetics, microRNAs and environment on developmental processes; 2) genome-wide studies; 3) novel imaging techniques for the study of gene expression and cellular function; 4) comparative genetics and genomics and 5) animal models of human genetic and developmental disorders. genesis presents reviews, full research articles, short research letters, and state-of-the-art technology reports that promote an understanding of the function of genes and the roles they play in complex developmental processes.
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