Old model [9], as well as the transformation model [5], would have predicted that the cloacal remnant is distribution broadly at the surface 
of the perineum. Both Six1 and Six2 are expressed in the PCM, but not ICM progenitors. Interestingly, Six1- and Six2- positive cell lineages contribute directly to perineum tissue. Furthermore, inducible genetic fate mapping demonstrates, for the first time, that Six2 expression in PCM progenitor contributes to the perineal stromal tissue, as early as e11.5. While the occlusion model does not exclude the possibility that ICM progenitors might also contribute to the perineum, these observations suggest that PCM progenitors are involved in perineum formation. Indeed, Six1 and Six2 double null mutants exhibit perineum agenesis defects. Taking together, we conclude that cloacal mesoderm progenitors are central to the separation of the urinary and digestive tracts, as well as to the outorder Gracillin growth and patterning of genital tubercle. We postulate that asymmetric growth causes narrowing of cloaca at the location marked by the cloacal membrane. The endodermal remnant is pushed to the midline epithelial surface of perineum between the anus and urethral meatus. We now refer to the morphogenesis event of the cloaca as “cloacal occlusion”. Since the term septation has between used in many developmental contexts, and implies explicitly the 
existence of a septum, which is still a mater of speculation during cloacal morphogenesis, we therefore prefer the use of the cloacal occlusion to describe the mechanism of cloacal division. This model provides a basicCloaca Septation and Urogenital Developmentframework, i.e. patterning along dorsoventral and rostrocaudal axes, with which to investigate normal and abnormal development of the anorectal and genitourinary structures.fluorescence dissection microscope equipped with a DP71 digital camera. Cryostat sections were used for TUNEL assays.Quantitative real-time PCR 125-65-5 price analysis Materials and Methods MiceAll animal studies were performed according to protocols reviewed and approved by the institutional animal care and use committee at the Children’s Hospital Boston. Six1 [12], Six2GCE/+, Six2GC/+ [14], R26RlacZ [15] mice have previously been reported. Genotyping of the mice was performed as described. For temporal induction of Cre recombination, tamoxifen (Sigma, T5648) was dissolved in sesame oil (Sigma, S3547) and administrated by intraperitioneal (IP) injection (50 g/kg body weight). Genital 15755315 tubercle tissue of e11.5 embryos was micro-dissected and snap-frozen on a dry ice/ethanol bath. RNA was purified based on manufacturer’s protocols (Qiagen RNAeasy mini). cDNA was synthesized using the Stratagene AccuscriptTM High Fidelity 1st strand cDNA synthesis (Agilent Technologies) using 200 ng of total RNA. Relative gene expression levels were normalized to an a-actin internal control, and analyzed using SYBR Green Master Mix (Affymetrix) on an ABI-7500 detector (Applied BioSystems). The following oligos were used: a-actin F: TCG TCG ACA ACG GCT CCG GCA TGT; a-actin R: CCA GCC AGG TCC AGA CGC AGG AT; Bmp4 F: GCC GAG CCA ACA CTG TGA GGA; Bmp4 R: GAT GCT GCT GAG GTT GAA GAG G; Bmp7 F: GGA GCG ATT TGA CAA CGA GAC C; Bmp7 R: AGT GGT TGC TGG TGG CTG TGA T; Msx1 F: AGG ACT CCT CAA GCT GCC AGA A; Msx1 R: CGG TTG GTC TTG TGC TTG CGT A; Fgf8 F: GGG AAG CTA ATT GCC AAG AG; Fgf8 R: TGT ACC AGC CCT CGT ACT TG; Fgf10 F: GCC ACC AAC TGC TCTT CTT C; Fgf10 R: CTG ACC TTG CCG TTC TTC TC; Dkk1 F: AT.Old model [9], as well as the transformation model [5], would have predicted that the cloacal remnant is distribution broadly at the surface of the perineum. Both Six1 and Six2 are expressed in the PCM, but not ICM progenitors. Interestingly, Six1- and Six2- positive cell lineages contribute directly to perineum tissue. Furthermore, inducible genetic fate mapping demonstrates, for the first time, that Six2 expression in PCM progenitor contributes to the perineal stromal tissue, as early as e11.5. While the occlusion model does not exclude the possibility that ICM progenitors might also contribute to the perineum, these observations suggest that PCM progenitors are involved in perineum formation. Indeed, Six1 and Six2 double null mutants exhibit perineum agenesis defects. Taking together, we conclude that cloacal mesoderm progenitors are central to the separation of the urinary and digestive tracts, as well as to the outgrowth and patterning of genital tubercle. We postulate that asymmetric growth causes narrowing of cloaca at the location marked by the cloacal membrane. The endodermal remnant is pushed to the midline epithelial surface of perineum between the anus and urethral meatus. We now refer to the morphogenesis event of the cloaca as “cloacal occlusion”. Since the term septation has between used in many developmental contexts, and implies explicitly the existence of a septum, which is still a mater of speculation during cloacal morphogenesis, we therefore prefer the use of the cloacal occlusion to describe the mechanism of cloacal division. This model provides a basicCloaca Septation and Urogenital Developmentframework, i.e. patterning along dorsoventral and rostrocaudal axes, with which to investigate normal and abnormal development of the anorectal and genitourinary structures.fluorescence dissection microscope equipped with a DP71 digital camera. Cryostat sections were used for TUNEL assays.Quantitative real-time PCR analysis Materials and Methods MiceAll animal studies were performed according to protocols reviewed and approved by the institutional animal care and use committee at the Children’s Hospital Boston. Six1 [12], Six2GCE/+, Six2GC/+ [14], R26RlacZ [15] mice have previously been reported. Genotyping of the mice was performed as described. For temporal induction of Cre recombination, tamoxifen (Sigma, T5648) was dissolved in sesame oil (Sigma, S3547) and administrated by intraperitioneal (IP) injection (50 g/kg body weight). Genital 15755315 tubercle tissue of e11.5 embryos was micro-dissected and snap-frozen on a dry ice/ethanol bath. RNA was purified based on manufacturer’s protocols (Qiagen RNAeasy mini). cDNA was synthesized using the Stratagene AccuscriptTM High Fidelity 1st strand cDNA synthesis (Agilent Technologies) using 200 ng of total RNA. Relative gene expression levels were normalized to an a-actin internal control, and analyzed using SYBR Green Master Mix (Affymetrix) on an ABI-7500 detector (Applied BioSystems). The following oligos were used: a-actin F: TCG TCG ACA ACG GCT CCG GCA TGT; a-actin R: CCA GCC AGG TCC AGA CGC AGG AT; Bmp4 F: GCC GAG CCA ACA CTG TGA GGA; Bmp4 R: GAT GCT GCT GAG GTT GAA GAG G; Bmp7 F: GGA GCG ATT TGA CAA CGA GAC C; Bmp7 R: AGT GGT TGC TGG TGG CTG TGA T; Msx1 F: AGG ACT CCT CAA GCT GCC AGA A; Msx1 R: CGG TTG GTC TTG TGC TTG CGT A; Fgf8 F: GGG AAG CTA ATT GCC AAG AG; Fgf8 R: TGT ACC AGC CCT CGT ACT TG; Fgf10 F: GCC ACC AAC TGC TCTT CTT C; Fgf10 R: CTG ACC TTG CCG TTC TTC TC; Dkk1 F: AT.
