Indian Institute of Science Education and Research (IISER, Pune), Dr. Homi Bhabha Road, Pune, Maharashtra, 411 008, India.
Mol Genet Genomics. 2019 Jun;294(3):583-596. doi: 10.1007/s00438-019-01532-4. Epub 2019 Jan 28.
The gametophyte of moss exhibits a simple body plan, yet its growth is regulated by complex developmental phenomena similar to angiosperms. Because moss can be easily maintained under laboratory conditions, amenable for gene targeting and the availability of genome sequence, P. patens has become an attractive model system for studying evolutionary traits. Until date, there has been no Agrobacterium-mediated Tnt1 mutagenesis protocol for haploid protonemal filaments of moss. Hence, we attempted to use the intact tobacco Tnt1 retrotransposon as a mutagen for P. patens. Bioinformatic analysis of initiator methionyl-tRNA (Met-tRNA), a critical host factor for Tnt1 transposition process, suggested that it can be explored as a mutagen for bryophytes. Using protonemal filaments and Agrobacterium-mediated transformation, 75 Tnt1 mutants have been generated and cryopreserved. SSAP analysis and TAIL-PCR revealed that Tnt1 is functional in P. patens and has a high-preference for gene and GC-rich regions. In addition, LTR::GUS lines exhibited a basal but tissue-specific inducible expression pattern. Forward genetic screen resulted in 5 novel phenotypes related to hormonal and gravity response, phyllid, and gamete development. SSAP analysis suggests that the Tnt1 insertion pattern is stable under normal growth conditions and the high-frequency phenotypic deviations are possibly due to the combination of haploid explant (protonema) and the choice of mutagen (Tnt1). We demonstrate that Agrobacterium-mediated Tnt1 insertional mutagenesis could generate stable P. patens mutant populations for future forward genetic studies.
藓类植物的配子体呈现出简单的身体结构,但它的生长受到复杂的发育现象的调节,这些现象与被子植物相似。由于藓类植物可以在实验室条件下很容易地维持,并且易于进行基因靶向和基因组序列的可用性,因此 P. patens 已成为研究进化特征的有吸引力的模式系统。迄今为止,还没有用于藓类植物单倍体原丝体的农杆菌介导的 Tnt1 诱变协议。因此,我们试图使用完整的烟草 Tnt1 反转录转座子作为 P. patens 的诱变剂。起始甲硫氨酸-tRNA(Met-tRNA)的生物信息学分析,Tnt1 转座过程的关键宿主因素,表明它可以作为苔藓植物的诱变剂进行探索。使用原丝体和农杆菌介导的转化,已经生成并冷冻保存了 75 个 Tnt1 突变体。SSAP 分析和 TAIL-PCR 表明 Tnt1 在 P. patens 中具有功能,并且对基因和 GC 丰富区域具有高偏好性。此外,LTR::GUS 系表现出基础但组织特异性的诱导表达模式。正向遗传筛选导致与激素和重力反应、叶状体和配子体发育相关的 5 种新表型。SSAP 分析表明,Tnt1 插入模式在正常生长条件下稳定,高频表型偏差可能是由于单倍体外植体(原丝体)和诱变剂(Tnt1)的选择的组合所致。我们证明,农杆菌介导的 Tnt1 插入诱变可以为未来的正向遗传研究生成稳定的 P. patens 突变体群体。