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非洲爪蟾一个混合基因的小鼠和人类同源基因的克隆、表达分析及染色体定位

Cloning, expression analysis, and chromosomal localization of murine and human homologues of a Xenopus mix gene.

作者信息

Robb L, Hartley L, Begley C G, Brodnicki T C, Copeland N G, Gilbert D J, Jenkins N A, Elefanty A G

机构信息

The Walter and Eliza Hall Institute of Medical Research, PO Royal Melbourne Hospital, Victoria, Australia.

出版信息

Dev Dyn. 2000 Dec;219(4):497-504. doi: 10.1002/1097-0177(2000)9999:9999<::AID-DVDY1070>3.0.CO;2-O.

Abstract

We report the cloning and chromosomal localization of murine and human Mix genes, members of a subclass of paired-like homeobox genes of which the Xenopus laevis Mix.1 gene is the founding member. The murine Mix gene was mapped to the distal region of chromosome 1 and the human region to the syntenic region 1q41-42. Northern analysis and RT-PCR of murine adult and embryonic tissues demonstrated that Mix expression was restricted to the early embryo. Whole-mount in situ hybridization revealed patchy but symmetrical Mix expression in visceral endoderm of embryonic day (E)5.5 embryos. In slightly older embryos, the expression was skewed to one side of the embryo and by E6.5, at the onset of gastrulation, expression was seen in the epiblast, visceral endoderm, nascent mesoderm, and the primitive streak. This expression pattern was maintained in mid- and late-streak embryos. In early bud-stage embryos, expression was strongest in the proximal two thirds of the streak, extending to the base of the allantois. By the headfold-stage, expression was confined to the remnant of the primitive streak in the caudal region of the embryo and, after E8.0, in the caudal notochord and tail bud mesoderm. Mix transcripts were no longer detectable after embryonic day 9.5.

摘要

我们报告了小鼠和人类Mix基因的克隆及染色体定位,Mix基因是配对样同源框基因亚类的成员,其中非洲爪蟾Mix.1基因是该亚类的首个成员。小鼠Mix基因定位于1号染色体的远端区域,人类Mix基因定位于同线性区域1q41 - 42。对小鼠成年和胚胎组织进行的Northern分析及逆转录聚合酶链反应(RT-PCR)表明,Mix表达仅限于早期胚胎。整体原位杂交显示,在胚胎第(E)5.5天胚胎的脏内胚层中,Mix表达呈斑片状但对称。在稍大一些的胚胎中,表达偏向胚胎的一侧,到E6.5,即原肠胚形成开始时,在胚盘、脏内胚层、新生中胚层和原条中可见表达。这种表达模式在原条中期和后期胚胎中得以维持。在早期芽阶段胚胎中,表达在原条近端三分之二处最强,延伸至尿囊基部。到头褶阶段,表达局限于胚胎尾部区域的原条残余部分,在E8.0之后,表达于尾部脊索和尾芽中胚层。在胚胎第9.5天之后,不再能检测到Mix转录本。

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