Bürglin Thomas R, Affolter Markus
Biozentrum, University of Basel, Klingelbergstrasse 50/70, 4056, Basel, Switzerland.
Department of Biomedicine, University of Basel, Mattenstrasse 28, 4058, Basel, Switzerland.
Chromosoma. 2016 Jun;125(3):497-521. doi: 10.1007/s00412-015-0543-8. Epub 2015 Oct 13.
Here, we provide an update of our review on homeobox genes that we wrote together with Walter Gehring in 1994. Since then, comprehensive surveys of homeobox genes have become possible due to genome sequencing projects. Using the 103 Drosophila homeobox genes as example, we present an updated classification. In animals, there are 16 major classes, ANTP, PRD, PRD-LIKE, POU, HNF, CUT (with four subclasses: ONECUT, CUX, SATB, and CMP), LIM, ZF, CERS, PROS, SIX/SO, plus the TALE superclass with the classes IRO, MKX, TGIF, PBC, and MEIS. In plants, there are 11 major classes, i.e., HD-ZIP (with four subclasses: I to IV), WOX, NDX, PHD, PLINC, LD, DDT, SAWADEE, PINTOX, and the two TALE classes KNOX and BEL. Most of these classes encode additional domains apart from the homeodomain. Numerous insights have been obtained in the last two decades into how homeodomain proteins bind to DNA and increase their specificity by interacting with other proteins to regulate cell- and tissue-specific gene expression. Not only protein-DNA base pair contacts are important for proper target selection; recent experiments also reveal that the shape of the DNA plays a role in specificity. Using selected examples, we highlight different mechanisms of homeodomain protein-DNA interaction. The PRD class of homeobox genes was of special interest to Walter Gehring in the last two decades. The PRD class comprises six families in Bilateria, and tinkers with four different motifs, i.e., the PAIRED domain, the Groucho-interacting motif EH1 (aka Octapeptide or TN), the homeodomain, and the OAR motif. Homologs of the co-repressor protein Groucho are also present in plants (TOPLESS), where they have been shown to interact with small amphipathic motives (EAR), and in yeast (TUP1), where we find an EH1-like motif in MATα2.
在此,我们更新了1994年与沃尔特·格林(Walter Gehring)共同撰写的关于同源异型基因的综述。自那时以来,由于基因组测序项目,对同源异型基因进行全面调查已成为可能。以103个果蝇同源异型基因为例,我们给出了一个更新的分类。在动物中,有16个主要类别,即ANTP、PRD、PRD-LIKE、POU、HNF、CUT(有四个亚类:ONECUT、CUX、SATB和CMP)、LIM、ZF、CERS、PROS、SIX/SO,以及包含IRO、MKX、TGIF、PBC和MEIS等类别的TALE超类。在植物中,有11个主要类别,即HD-ZIP(有四个亚类:I至IV)、WOX、NDX、PHD、PLINC、LD、DDT、SAWADEE、PINTOX,以及两个TALE类别KNOX和BEL。这些类别中的大多数除了同源异型域外还编码其他结构域。在过去二十年中,关于同源异型域蛋白如何与DNA结合并通过与其他蛋白相互作用增加其特异性以调节细胞和组织特异性基因表达,已获得了许多见解。不仅蛋白质-DNA碱基对接触对于正确的靶标选择很重要;最近的实验还表明,DNA的形状在特异性方面也起作用。通过选定的例子,我们突出了同源异型域蛋白与DNA相互作用的不同机制。在过去二十年中,同源异型基因的PRD类别引起了沃尔特·格林的特别关注。PRD类别在两侧对称动物中包括六个家族,并涉及四种不同的基序,即配对结构域、与Groucho相互作用的基序EH1(又名八肽或TN)、同源异型域和OAR基序。共抑制蛋白Groucho的同源物在植物(TOPLESS)中也存在,在那里它们已被证明与小的两亲性基序(EAR)相互作用,在酵母(TUP1)中也存在,在MATα2中我们发现了一个类似EH1的基序。