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FIGURE 3. Cdx2-deficient cells maintain developmental potential but are unable to implant after nuclear transfer.

From the following article:

Generation of nuclear transfer-derived pluripotent ES cells from cloned Cdx2-deficient blastocysts

Alexander Meissner and Rudolf Jaenisch

Nature 439, 212-215(12 January 2006)

doi:10.1038/nature04257

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a, b, In each example shown, five nuclear transfer blastocysts were transferred at day 3.5 into the uterus of a day 2.5 pseudo-pregnant female. a, Cdx2-deficient blastocysts fail to implant. A representative uterus isolated at day 6.5 is shown. No deciduae were detectable from transplanted Cdx2-deficient blastocysts. b, Control nuclear transfer blastocysts showed normal implantation sites at day 6.5. c, Bright-field image of a postnatal Cdx22Lox ES chimaera. d, GFP signal indicates a contribution from Cdx22Lox ES cells. eg, Histological sections and anti-GFP staining from a newborn Cdx22Lox chimaera. There was a contribution to the liver (endoderm; e) and muscle (mesoderm; f) but not to the intestine (g). h, Anti-Cdx2 staining of the intestine shown in g. i, Coat colour contribution of Cdx22Lox ES cells. Recipient blastocysts have a C57BL/6 times DBA/2 F1 background and the Cdx22Lox ES cells a C57BL/6 times 129SvJae background. The presence of agouti (129/SvJae) fur indicates donor cell contribution. A litter with one wild type (black mouse below the top agouti), two low-contribution (middle) and two high-contribution chimaeras are shown.

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