George Janet A, DeBaryshe P Gregory, Traverse Karen L, Celniker Susan E, Pardue Mary-Lou
Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, USA.
Genome Res. 2006 Oct;16(10):1231-40. doi: 10.1101/gr.5348806. Epub 2006 Sep 8.
The emerging sequence of the heterochromatic portion of the Drosophila melanogaster genome, with the most recent update of euchromatic sequence, gives the first genome-wide view of the chromosomal distribution of the telomeric retrotransposons, HeT-A, TART, and Tahre. As expected, these elements are entirely excluded from euchromatin, although sequence fragments of HeT-A and TART 3 untranslated regions are found in nontelomeric heterochromatin on the Y chromosome. The proximal ends of HeT-A/TART arrays appear to be a transition zone because only here do other transposable elements mix in the array. The sharp distinction between the distribution of telomeric elements and that of other transposable elements suggests that chromatin structure is important in telomere element localization. Measurements reported here show (1) D. melanogaster telomeres are very long, in the size range reported for inbred mouse strains (averaging 46 kb per chromosome end in Drosophila stock 2057). As in organisms with telomerase, their length varies depending on genotype. There is also slight under-replication in polytene nuclei. (2) Surprisingly, the relationship between the number of HeT-A and TART elements is not stochastic but is strongly correlated across stocks, supporting the idea that the two elements are interdependent. Although currently assembled portions of the HeT-A/TART arrays are from the most-proximal part of long arrays, approximately 61% of the total HeT-A sequence in these regions consists of intact, potentially active elements with little evidence of sequence decay, making it likely that the content of the telomere arrays turns over more extensively than has been thought.
黑腹果蝇基因组异染色质部分的最新测序结果,结合常染色质序列的最新更新,首次提供了全基因组范围内端粒逆转座子HeT - A、TART和Tahre染色体分布的视图。正如预期的那样,这些元件完全被排除在常染色质之外,尽管在Y染色体的非端粒异染色质中发现了HeT - A和TART 3'非翻译区的序列片段。HeT - A/TART阵列的近端似乎是一个过渡区,因为只有在这里其他转座元件才会混入阵列中。端粒元件与其他转座元件分布的明显区别表明染色质结构在端粒元件定位中很重要。此处报道的测量结果表明:(1)黑腹果蝇的端粒非常长,处于报道的近交小鼠品系的大小范围内(果蝇品系2057中每条染色体末端平均为46 kb)。与具有端粒酶的生物体一样,它们的长度因基因型而异。在多线核中也存在轻微的复制不足。(2)令人惊讶的是,HeT - A和TART元件数量之间的关系不是随机的,而是在不同品系间强烈相关,这支持了这两个元件相互依赖的观点。尽管目前组装的HeT - A/TART阵列部分来自长阵列的最近端部分,但这些区域中约61%的HeT - A总序列由完整的、可能具有活性的元件组成,几乎没有序列衰减的证据,这使得端粒阵列的内容物比之前认为的更广泛地更新换代。