Resequencing of the TMF-1 (TATA Element Modulatory Factor) regulated protein (TRNP1) gene in domestic and wild canids.

James C Sacco, Emma Starr, Alyssa Weaver, Rachel Dietz, Muhammad A Spocter
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Abstract

Background: Cortical folding is related to the functional organization of the brain. The TMF-1 regulated protein (TRNP1) regulates the expansion and folding of the mammalian cerebral cortex, a process that may have been accelerated by the domestication of dogs. The objectives of this study were to sequence the TRNP1 gene in dogs and related canid species, provide evidence of its expression in dog brain and compare the genetic variation within dogs and across the Canidae. The gene was located in silico to dog chromosome 2. The sequence was experimentally confirmed by amplifying and sequencing the TRNP1 exonic and promoter regions in 72 canids (36 purebred dogs, 20 Gy wolves and wolf-dog hybrids, 10 coyotes, 5 red foxes and 1 Gy fox).

Results: A partial TRNP1 transcript was isolated from several regions in the dog brain. Thirty genetic polymorphisms were found in the Canis sp. with 17 common to both dogs and wolves, and only one unique to dogs. Seven polymorphisms were observed only in coyotes. An additional 9 variants were seen in red foxes. Dogs were the least genetically diverse. Several polymorphisms in the promoter and 3'untranslated region were predicted to alter TRNP1 function by interfering with the binding of transcriptional repressors and miRNAs expressed in neural precursors. A c.259_264 deletion variant that encodes a polyalanine expansion was polymorphic in all species studied except for dogs. A stretch of 15 nucleotides that is found in other mammalian sequences (corresponding to 5 amino acids located between Pro58 and Ala59 in the putative dog protein) was absent from the TRNP1 sequences of all 5 canid species sequenced. Both of these aforementioned coding sequence variations were predicted to affect the formation of alpha helices in the disordered region of the TRNP1 protein.

Conclusions: Potentially functionally important polymorphisms in the TRNP1 gene are found within and across various Canis species as well as the red fox, and unique differences in protein structure have evolved and been conserved in the Canidae compared to all other mammalian species.

家犬和野生犬TMF-1 (TATA元件调节因子)调节蛋白(TRNP1)基因重测序
背景:皮层折叠与大脑的功能组织有关。TMF-1调节蛋白(TRNP1)调节哺乳动物大脑皮层的扩张和折叠,这一过程可能因驯化狗而加速。本研究的目的是对狗和相关犬科动物的TRNP1基因进行测序,提供其在狗脑中的表达证据,并比较狗和犬科动物之间的遗传变异。该基因位于狗的2号染色体上。通过对72种犬科动物(36只纯种犬、20只灰狼和灰狗杂种、10只土狼、5只红狐和1只灰狐)的TRNP1外显子和启动子区域进行扩增和测序,实验证实了该序列。结果:从狗脑的几个区域分离出部分TRNP1转录物。在犬科动物中发现了30种遗传多态性,其中17种是狗和狼共有的,只有一种是狗所特有的。7个多态性仅在土狼中观察到。在红狐身上还发现了另外9种变异。狗的基因多样性最低。据预测,启动子和3'非翻译区的一些多态性通过干扰转录抑制因子和神经前体中表达的mirna的结合来改变TRNP1的功能。编码聚丙氨酸扩增的c.259_264缺失变异在除狗外的所有研究物种中都是多态的。在所有5种犬科动物的TRNP1序列中都没有发现在其他哺乳动物序列中发现的15个核苷酸(对应于假定的狗蛋白中位于Pro58和Ala59之间的5个氨基酸)。据预测,上述两种编码序列变异都会影响TRNP1蛋白紊乱区域α螺旋的形成。结论:TRNP1基因具有潜在的重要功能的多态性,在不同的犬科动物和红狐中被发现,与所有其他哺乳动物相比,犬科动物在蛋白质结构上的独特差异已经进化并被保存下来。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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