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X染色体上同源区段内基因顺序的部分倒位。

Partial inversion of gene order within a homologous segment on the X chromosome.

作者信息

Laval S H, Boyd Y

机构信息

Genetics Division, Medical Research Council Radiobiology Unit, Didcot, Oxon, UK.

出版信息

Mamm Genome. 1993;4(2):119-23. doi: 10.1007/BF00290437.

Abstract

The locus for the erthyroid transcription factor, GATA1, has been positioned in the small interval between DXS255 and TIMP on the proximal short arm of the human X Chromosome (Chr) by use of a partial human cDNA clone and a well-characterized somatic cell hybrid panel. Analysis of selected recombinants from 108 Mus musculus x Mus spretus backcross progeny with the same clone confirmed that the homologous murine locus (Gf-1) lies between Otc and the centromere of the mouse X Chr. These data imply that a partial inversion of gene order has occurred within the conserved segment that represents Xp21.1-Xp11.23 in human (CYBB-GATA1) and the proximal 6 cM of the mouse X Chr (Gf-1-Timp). Furthermore, they indicate that the mouse mutant scurfy and the human genetic disorder Wiskott-Aldrich syndrome, which have been mapped to the same regions as GATA1/Gf-1 in both species, may indeed be homologous disorders.

摘要

利用一个部分人类cDNA克隆和一个特征明确的体细胞杂交板,已将红细胞转录因子GATA1的基因座定位在人类X染色体(Chr)近端短臂上DXS255和TIMP之间的小间隔内。用同一克隆对108只小家鼠× 西班牙小鼠回交后代中的选定重组体进行分析,证实同源鼠基因座(Gf-1)位于Otc和小鼠X Chr的着丝粒之间。这些数据表明,在代表人类Xp21.1-Xp11.23(CYBB-GATA1)和小鼠X Chr近端6 cM(Gf-1-Timp)的保守区段内发生了基因顺序的部分倒位。此外,它们表明,已在两个物种中定位到与GATA1/Gf-1相同区域的小鼠突变体scurfy和人类遗传疾病威斯科特-奥尔德里奇综合征可能确实是同源疾病。

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