Computational Evolutionary Genomics Lab, Department of Biological Sciences, IISER Bhopal, Bhauri, Madhya Pradesh, India.
Immunogenetics. 2020 Dec;72(9-10):507-515. doi: 10.1007/s00251-020-01186-2. Epub 2020 Nov 28.
The loss of conserved genes has the potential to alter phenotypes drastically. Screening of vertebrate genomes for lineage-specific gene loss events has identified numerous natural knockouts associated with specific phenotypes. We provide evidence for the loss of a multi-exonic plasminogen receptor KT (PLGRKT) protein-encoding gene located on the Z chromosome in chicken. Exons 1 and 2 are entirely missing; remnants of exon 3 and a mostly intact exon 4 are identified in an assembly gap-free region in chicken with conserved synteny across species and verified using transcriptome and genome sequencing. PLGRKT gene disrupting changes are present in representative species from all five galliform families. In contrast to this, the presence of an intact transcriptionally active PLGRKT gene in species such as mallard, swan goose, and Anolis lizard suggests that gene loss occurred in the galliform lineage sometime between 68 and 80 Mya. The presence of galliform specific chicken repeat 1 (CR1) insertion at the erstwhile exon 2 of PLGRKT gene suggests repeat insertion-mediated loss. However, at least nine other independent PLGRKT coding frame disrupting changes in other bird species are supported by genome sequencing and indicate a role for relaxed purifying selection before CR1 insertion. The recurrent loss of a conserved gene with a role in the regulation of macrophage migration, efferocytosis, and blood coagulation is intriguing. Hence, we propose potential candidate genes that might be compensating the function of PLGRKT based on the presence of a C-terminal lysine residue, transmembrane domains, and gene expression patterns.
保守基因的丢失有可能极大地改变表型。通过对脊椎动物基因组进行谱系特异性基因丢失事件的筛选,已经确定了许多与特定表型相关的自然敲除。我们提供了鸡 Z 染色体上多外显子纤溶酶原受体 KT(PLGRKT)蛋白编码基因丢失的证据。外显子 1 和 2 完全缺失;在鸡的一个组装无间隙区域中鉴定出了外显子 3 的残留物和大部分完整的外显子 4,该区域在物种间具有保守的同线性,并使用转录组和基因组测序进行了验证。PLGRKT 基因破坏变化存在于来自所有五个鹑形目家族的代表性物种中。与此相反,在像野鸭、鹅和蜥蜴等物种中存在完整的转录活性 PLGRKT 基因,这表明基因丢失发生在 68 到 80 百万年前的鹑形目谱系中。鹑形目特异性鸡重复 1(CR1)插入到 PLGRKT 基因的原外显子 2 中,表明重复插入介导的丢失。然而,在其他鸟类物种中,至少有九个其他独立的 PLGRKT 编码框架破坏变化得到了基因组测序的支持,并表明在 CR1 插入之前存在放松的纯化选择。保守基因的反复丢失,该基因在调节巨噬细胞迁移、吞噬作用和血液凝固方面发挥作用,这很有趣。因此,我们根据 C 末端赖氨酸残基、跨膜结构域和基因表达模式的存在,提出了可能补偿 PLGRKT 功能的潜在候选基因。