Dekel Yaron, Machluf Yossy, Ben-Dor Shifra, Yifa Oren, Stoler Aviad, Ben-Shlomo Izhar, Bercovich Dani
MIGAL - Galilee Research Institute, Kiryat Shmona, Israel.
Tel Hai College, Upper Galilee, Israel.
BMC Genomics. 2015 Feb 5;16(1):53. doi: 10.1186/s12864-015-1235-8.
In recent years, the perception of transposable genetic elements has changed from "junk DNA" to a focus of interest when appearing near or inside genes. Bov-A2 is a short interspersed nuclear element (SINE) that was first found in Bovidae and later in other ruminants. This retroposon is mostly used as a marker for phylogenetic analysis.
We describe insertions of Bov-A2 in the promoter region of TP53, a key tumor suppressor gene that is indispensable for diverse developmental processes, in Antilopinae and Tragelaphini (belonging to the Bovinae subfamily). In Tragelaphini two Bov-A2 elements were inserted sequentially, whereas in 5 tribes of Antilopinae only one Bov-A2 element was inserted, in a different site and reverse orientation. The entrance site in both cases employed short palindromes that can form hairpin secondary structures. Interestingly, mutations that create or disrupt base pairing in the palindrome sequence dictated the presence or absence of Bov-A2, such as in the domestic cow and buffalo, which lack Bov-A2. Transcription factor binding site analysis revealed unique binding sites for STAT3 and NFκB within the Bov-A2 sequence, which together with TP53 itself are known to play a crucial role in mammary involution.
This report demonstrates how short palindromes serve as hot spots for Bov-A2 retroposon insertion into the mammalian genome. The strict correlation between point mutation in the palindromes and the presence/absence of Bov-A2 retroposon insertions, questions the use of singular insertion events as valid phylogenetic markers inside families. Bov-A2 insertion into the TP53 promoter in Antilopinae and Tragelaphini may not only provide a genetic network that regulates mammary involution, but can also answer the need for rapid mammary involution in Savanna antelopes after weaning, partially in response to predation stress. The absence of Bov-A2 in domestic bovids may constitute the molecular background for greater lactation persistency.
近年来,人们对转座遗传元件的认知已从“垃圾DNA”转变为当出现在基因附近或内部时成为关注焦点。Bov-A2是一种短散在核元件(SINE),最初在牛科动物中发现,后来在其他反刍动物中也有发现。这种逆转座子大多用作系统发育分析的标记。
我们描述了Bov-A2在羚羊亚科和薮羚亚科(属于牛亚科)的TP53启动子区域的插入情况,TP53是一个关键的肿瘤抑制基因,对多种发育过程不可或缺。在薮羚亚科中,两个Bov-A2元件依次插入,而在羚羊亚科的5个部落中,只有一个Bov-A2元件插入,且插入位点不同,方向相反。两种情况下的插入位点都利用了能形成发夹二级结构的短回文序列。有趣的是,在回文序列中产生或破坏碱基配对的突变决定了Bov-A2的存在与否,比如家牛和水牛就缺乏Bov-A2。转录因子结合位点分析揭示了Bov-A2序列内STAT3和NFκB的独特结合位点,已知这些位点与TP53自身一起在乳腺退化中起关键作用。
本报告展示了短回文序列如何成为Bov-A2逆转座子插入哺乳动物基因组的热点。回文序列中的点突变与Bov-A2逆转座子插入的存在与否之间的严格相关性,对将单个插入事件用作科内有效系统发育标记的做法提出了质疑。Bov-A2插入羚羊亚科和薮羚亚科的TP53启动子不仅可能提供一个调节乳腺退化的遗传网络,还能满足稀树草原羚羊断奶后快速乳腺退化的需求,部分原因是应对捕食压力。家养牛科动物中缺乏Bov-A2可能构成了泌乳持续性更强的分子背景。