Analysis of L1-chimeric transcripts derived from bidirectional promoter of human-specific L1

被引:3
|
作者
Kim, Songmi [1 ,2 ]
Kim, Yun-Ji [1 ,2 ]
Han, Kyudong [1 ,2 ]
机构
[1] Dankook Univ, Dept Nanobiomed Sci, Cheonan 330714, South Korea
[2] Dankook Univ, PLUS NBM Global Res Ctr Regenerat Med BK21, Cheonan 330714, South Korea
关键词
Alternative splicing; Human-specific LINE-1 (L1); L1-chimeric transcript; Promoter; TRANSPOSABLE ELEMENTS; ANTISENSE PROMOTER; FAMILY; RETROTRANSPOSONS; IDENTIFICATION; IMPACT;
D O I
10.1007/s13258-015-0363-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
LINE-1s (L1s) have contributed to gene structure variation and they can affect the expression of nearby genes in the human genome. Here, we collected 35 human-specific L1s that may play a role as alternative promoters. In addition, we identified 54 L1-chimeric transcripts generated from these L1s using bioinformatics' tools and carried out reverse transcription-PCR to analyze their expressional pattern in 20 human normal tissues and 9 human cancer tissues. Consequently, 30 L1-chimeric transcripts were experimentally confirmed. Most L1-chimeric transcripts were broadly expressed. Interestingly, we found that EST CD709363 derived from C14orf37 gene was expressed in trachea only among normal tissues, but it was expressed in several cancer tissues including brain, lung, skin, and esophagus. We also newly identified three alternative transcripts, which were not in the UCSC genome database. One alternative transcript was derived from RABGAP1L gene and the other two transcripts were from CAMK4 gene. In addition, we analyzed putative transcription binding sites within the four L1s located in the promoter region. These had several transcription factor binding sites related to promoters. Our results show that human-specific L1s could contribute to human transcriptome diversity and transcriptional gene expression in different types of human tissues.
引用
收藏
页码:69 / 79
页数:11
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