College of Animal Science, Henan Agricultural University, Zhengzhou, 450002 Henan, People's Republic of China.
Mol Biol Rep. 2011 Oct;38(7):4397-403. doi: 10.1007/s11033-010-0567-3. Epub 2010 Dec 15.
Lmbr1 is the key candidate gene for limb development. Until now, at least five and four alternative splicing isoforms of Lmbr1 gene have been found in human and mouse, respectively. However, only two alternative splicing isoforms of this homologous gene have been reported in chicken. In the present study, one novel chicken Lmbr1 transcript variant (designated Lmbr1-1) was identified by 5' RACE and RT-PCR. Chicken Lmbr1-1 possesses one novel transcription start site different from Lmbr1-N, and was predicted to encode one 192 amino acid protein with length variation in comparison with chicken LMBR1-N protein, which was produced by 5' spliced site variation of chicken Lmbr1-N exon 10. Comparing with Lmbr1-N transcript, chicken Lmbr1-1 exhibited restricted tissue distribution of the expression. Comparative sequence analysis revealed a highly conservative intron element between chicken and mammalians from the intron 9 of chicken Lmbr1-N, indicating their possible importance as intronic elements in the regulation of alternative splicing of Lmbr1 in vertebrates. By direct PCR sequencing the exon 10 and its flanking sequences in chicken Lmbr1-N, four variation sites/haplotypes were identified from six chicken breeds. One 797A/G nonsynonymous mutation (266Arg/Gln) locating in exon 10 of chicken Lmbr1-N was predicted to affect the exon splice enhancer motif for serine/arginine-rich protein recognition. These data demonstrated that chicken Lmbr1 was alternatively spliced to generate multiple splice forms, as was the case in mammals and each of the alternative splicing isoforms might function differentially.
Lmbr1 是肢体发育的关键候选基因。到目前为止,在人类和小鼠中分别发现了至少五个和四个 Lmbr1 基因的选择性剪接异构体。然而,在鸡中仅报道了这个同源基因的两个选择性剪接异构体。在本研究中,通过 5' RACE 和 RT-PCR 鉴定了一个新的鸡 Lmbr1 转录变体(命名为 Lmbr1-1)。鸡 Lmbr1-1 具有一个与 Lmbr1-N 不同的新型转录起始位点,并且预测编码一种 192 个氨基酸的蛋白质,与鸡 LMBR1-N 蛋白相比长度发生变化,这是由于鸡 Lmbr1-N 外显子 10 的 5'剪接位点变化所致。与 Lmbr1-N 转录本相比,鸡 Lmbr1-1 的表达具有受限的组织分布。比较序列分析显示,鸡 Lmbr1-N 的内含子 9 中存在一个高度保守的内含子元件,这表明它们可能作为脊椎动物 Lmbr1 选择性剪接的内含子元件具有重要作用。通过直接 PCR 测序鸡 Lmbr1-N 的外显子 10 及其侧翼序列,从六个鸡品种中鉴定出四个变异位点/单倍型。一个位于鸡 Lmbr1-N 外显子 10 中的 797A/G 非同义突变(266Arg/Gln)预测会影响丝氨酸/精氨酸丰富蛋白识别的外显子剪接增强子基序。这些数据表明,鸡 Lmbr1 通过选择性剪接产生多种剪接形式,与哺乳动物的情况一样,每个选择性剪接异构体可能具有不同的功能。