首页> 外文期刊>Somatic Cell and Molecular Genetics >TRANSCRIBED SEQUENCES ENCODED IN THE REGION INVOLVED IN CONTIGUOUS DELETION SYNDROME THAT COMPRISES - X-LINKED STAPES FIXATION AND DEAFNESS
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TRANSCRIBED SEQUENCES ENCODED IN THE REGION INVOLVED IN CONTIGUOUS DELETION SYNDROME THAT COMPRISES - X-LINKED STAPES FIXATION AND DEAFNESS

机译:包含在相邻的缺失综合征中的编码区域的翻译序列-X链球固定和缺失

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摘要

We have used a direct cDNA selection protocol to isolate expressed sequences from yeast artificial chromosome clones that contain approximately 900 Kb of genomic DNA from Xq21 band that is deleted in contiguous gene syndromes comprising of mixed deafness associated with stapes fixation (DFN3). In addition to identifying Brn4 (POU3f4), a POU domain containing transcription factor that is involved in DFN3 phenotype, we have isolated seven short fragment cDNAs mapping to the deleted region. Some of the selected fragments showed X-chromosome specificity and hybridized to autosomal DNA fragments, indicating the presence of a low abundance interspersed repent in the cDNAs or their homology to some uncharacterized family of genes. In conformity with the inertness of Xq21 band our results demonstrate that the region encodes far less than the average density of genes in other parts of the genome.
机译:我们已使用直接cDNA选择协议从酵母人工染色体克隆中分离表达序列,该克隆包含Xq21带中大约900 Kb的基因组DNA,并在连续基因综合征中缺失,该综合征包括与骨固定相关的混合性聋(DFN3)。除了鉴定Brn4(POU3f4)(一个包含与DFN3表型有关的转录因子的POU域)外,我们还分离了七个短片段cDNA,它们映射到缺失的区域。某些选定的片段显示X染色体特异性并与常染色体DNA片段杂交,表明cDNA中存在低丰度散布的re悔或它们与某些未表征的基因家族的同源性。与Xq21谱带的惰性一致,我们的结果表明该区域编码的基因远少于基因组其他部分中基因的平均密度。

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