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诺森(No-0)显著的花中花表型由一个新等位基因引起。

The Striking Flower-in-Flower Phenotype of Nossen (No-0) is Caused by a Novel Allele.

作者信息

Mohrholz Anne, Sun Hequan, Glöckner Nina, Hummel Sabine, Kolukisaoglu Üner, Schneeberger Korbinian, Harter Klaus

机构信息

Center for Plant Molecular Biology, Eberhard Karls University Tübingen, 72076 Tübingen, Germany.

Department of Plant Developmental Biology, Max Planck Institute for Plant Breeding Research, 50829 Cologne, Germany.

出版信息

Plants (Basel). 2019 Dec 13;8(12):599. doi: 10.3390/plants8120599.

Abstract

The transition to reproduction is a crucial step in the life cycle of any organism. In the establishment of reproductive growth can be divided into two phases: Firstly, cauline leaves with axillary meristems are formed and internode elongation begins. Secondly, lateral meristems develop into flowers with defined organs. Floral shoots are usually determinate and suppress the development of lateral shoots. Here, we describe a transposon insertion mutant in the Nossen accession with defects in floral development and growth. Most strikingly is the outgrowth of stems from the axillary bracts of the primary flower carrying secondary flowers. Therefore, we named this mutant flower-in-flower (). However, the transposon insertion in the annotated gene is not the cause for the phenotype. By means of classical and genome sequencing-based mapping, the mutation responsible for the phenotype was found to be in the gene. The mutation, a G-to-A exchange in the second exon of , creates a novel allele and results in a cysteine-to-tyrosine exchange in the α1-helix of LEAFY's DNA-binding domain. This exchange abolishes target DNA-binding, whereas subcellular localization and homomerization are not affected. To explain the strong fif phenotype against these molecular findings, several hypotheses are discussed.

摘要

向生殖阶段的转变是任何生物体生命周期中的关键一步。生殖生长的建立可分为两个阶段:首先,形成带有腋生分生组织的茎生叶,节间开始伸长。其次,侧生分生组织发育成具有特定器官的花。花茎通常是有限生长的,并抑制侧枝的发育。在这里,我们描述了一个诺森品种中的转座子插入突变体,其在花发育和生长方面存在缺陷。最显著的是,在携带次生花的初级花的腋生苞片处茎生长。因此,我们将这个突变体命名为花中花()。然而,注释基因中的转座子插入并非该表型的原因。通过经典的和基于基因组测序的定位,发现导致该表型的突变位于基因中。该突变是中的第二个外显子中的G到A的交换,产生了一个新的等位基因,并导致LEAFY DNA结合结构域的α1螺旋中的半胱氨酸到酪氨酸的交换。这种交换消除了对靶DNA的结合,而亚细胞定位和同源二聚化不受影响。为了解释针对这些分子发现的强烈的花中花表型,讨论了几种假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f183/6963406/84572d6d37c9/plants-08-00599-g001.jpg

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