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首页> 外文期刊>Developmental biology >Selective chromatid segregation mechanism proposed for the human split hand/foot malformation development by chromosome 2 translocations: A perspective
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Selective chromatid segregation mechanism proposed for the human split hand/foot malformation development by chromosome 2 translocations: A perspective

机译:为通过染色体2易位的人类分裂的手/脚畸形发展提出的选择性染色单体分离机制:一个角度

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Three unrelated chromosome 2q14.1-14.2 region translocations caused the split hand/foot limb malformation development in humans by an unknown mechanism. Their etiology was described by the autosomal dominant inheritance with incomplete penetrance genetic model although authors stated, "the understanding of the genotype-to-phenotype relationship has been most challenging". The conundrums are that no mutation was found in known genes located at or near the translocation breakpoints, some limbs were malformed while others were not in the same patient and surprisingly breakpoints lie at relatively large distance of more than 2.5 million bases to have caused disorder-causing gene mutations in a single gene. To help understand translocations etiology for limb development, we invoke the selective DNA strand/chromatid-specific epigenetic imprinting and segregation mechanism employed by the two highly diverged fission yeasts to produce daughter cells of different cell types by mitosis. By this mechanism, an anterior- and posterior-limb-tissues-generating pair of daughter cells is produced by a single deterministic cell dividing in the anlagen of the limb bud. Accordingly, malformation develops simply because translocations hinder the proper distribution of chromatid-specific epialleles of a limb developmental gene during the deterministic cell's mitosis. It is tempting to speculate that such a mechanism might involve the HOXD-cluster genes situated centromere-distal to the translocation breakpoints many million bases away at the 2q31.1 region. Further genetic tests of the hypothesis are proposed for the human and mouse limb development. In sum, genetic analysis of translocations suggests that the sequence asymmetry of strands in the double-helical DNA structure of a developmental gene forms the physical basis of daughter cells' developmental asymmetry, thus opposing the morphogen-gradient research paradigm of limb development. Published by Elsevier Inc.
机译:三个不相关的染色体2q14.1-14.2区域易位,是由未知机制导致人的手/足四肢畸形的发展。他们的病因通过不完全外显遗传模型的常染色体显性遗传来描述,尽管作者说:“对基因型与表型关系的理解是最具挑战性的”。难题在于,在易位断裂点或附近的已知基因中未发现突变,一些肢体畸形,而其他肢体不在同一患者中,而且令人惊讶的是,断裂点位于相对较大的距离(超过250万个碱基)而导致了疾病-导致单个基因发生基因突变。为了帮助理解易位病因肢体发育的原因,我们调用了选择性DNA链/染色单体特异的表观遗传印记和分离机制,该机制由两个高度分散的裂变酵母通过有丝分裂产生不同细胞类型的子代细胞。通过这种机制,通过在肢芽的胶原中分裂的单个确定性细胞产生一对产生前肢和后肢组织的子细胞。因此,畸形发展仅是因为易位阻碍了确定性细胞有丝分裂过程中肢体发育基因的染色单体特异性表位等位基因的正确分布。试图推测这种机制可能与位于2q31.1区域数百万个碱基向着丝点距离着丝点远的HOXD簇基因有关。该假说的进一步的遗传学测试被提出用于人类和小鼠肢体的发育。总之,易位的遗传分析表明,发育基因的双螺旋DNA结构中链的序列不对称形成了子细胞发育不对称的物理基础,从而与肢体发育的形态发生梯度研究范式相对立。由Elsevier Inc.发布

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