Wellcome Trust Sanger Institute, Hinxton, UK.
PLoS One. 2012;7(11):e51065. doi: 10.1371/journal.pone.0051065. Epub 2012 Nov 30.
Mutanlallemand (mtl) and Belly Spot and Deafness (bsd) are two new spontaneous alleles of the Lmx1a gene in mice. Homozygous mutants show head tossing and circling behaviour, indicative of vestibular defects, and they have short tails and white belly patches of variable size. The analysis of auditory brainstem responses (ABR) showed that mtl and bsd homozygotes are deaf, whereas heterozygous and wildtype littermates have normal hearing. Paint-filled inner ears at E16.5 revealed that mtl and bsd homozygotes lack endolymphatic ducts and semicircular canals and have short cochlear ducts. These new alleles show similarities with dreher (Lmx1a) mutants. Complementation tests between mtl and dreher and between mtl and bsd suggest that mtl and bsd are new mutant alleles of the Lmx1a gene. To determine the Lmx1a mutation in mtl and bsd mutant mice we performed PCR followed by sequencing of genomic DNA and cDNA. The mtl mutation is a single point mutation in the 3' splice site of exon 4 leading to an exon extension and the activation of a cryptic splice site 44 base pairs downstream, whereas the bsd mutation is a genomic deletion that includes exon 3. Both mutations lead to a truncated LMX1A protein affecting the homeodomain (mtl) or LIM2-domain (bsd), which is critical for LMX1A protein function. Moreover, the levels of Lmx1a transcript in mtl and bsd mutants are significantly down-regulated. Hmx2/3 and Pax2 expression are also down-regulated in mtl and bsd mutants, suggesting a role of Lmx1a upstream of these transcription factors in early inner ear morphogenesis. We have found that these mutants develop sensory patches although they are misshapen. The characterization of these two new Lmx1a alleles highlights the critical role of this gene in the development of the cochlea and vestibular system.
Mutanlallemand (mtl) 和腹部斑点和耳聋 (bsd) 是小鼠 Lmx1a 基因的两个新的自发等位基因。纯合突变体表现出头部摆动和盘旋行为,表明前庭缺陷,并且它们的尾巴短,腹部有大小不一的白色斑点。听觉脑干反应 (ABR) 的分析表明,mtl 和 bsd 纯合子是聋的,而杂合子和野生型同窝仔则具有正常听力。E16.5 时填充有油漆的内耳显示,mtl 和 bsd 纯合子缺乏内淋巴导管和半规管,并且耳蜗导管短。这些新的等位基因与 dreher (Lmx1a) 突变体相似。mtl 和 dreher 之间以及 mtl 和 bsd 之间的互补测试表明,mtl 和 bsd 是 Lmx1a 基因的新突变等位基因。为了确定 mtl 和 bsd 突变小鼠中的 Lmx1a 突变,我们进行了 PCR 后测序基因组 DNA 和 cDNA。mtl 突变是外显子 4 的 3' 剪接位点的单点突变,导致外显子延伸并激活下游 44 个碱基的隐性剪接位点,而 bsd 突变是包含外显子 3 的基因组缺失。这两种突变都导致 LMX1A 蛋白截断,影响同源域(mtl)或 LIM2 域(bsd),这对 LMX1A 蛋白功能至关重要。此外,mtl 和 bsd 突变体中的 Lmx1a 转录本水平显著下调。mtl 和 bsd 突变体中的 Hmx2/3 和 Pax2 表达也下调,表明 Lmx1a 在这些转录因子的早期内耳形态发生中起上游作用。我们发现这些突变体虽然形状不规则,但仍能发育出感觉斑块。这两个新的 Lmx1a 等位基因的特征突出了该基因在耳蜗和前庭系统发育中的关键作用。