Majewska Marta, Panasiewicz Grzegorz, Klisch Karl, Olivera Louis V M, Mamani Javier M, Abd-Elnaeim Mahmoud M, Szafranska Bozena
Department of Animal Physiology, University of Warmia and Mazury in Olsztyn, 10-719 Olsztyn-Kortowo, Oczapowskiego Str 1A/222, Poland.
Reprod Biol. 2009 Jul;9(2):127-50. doi: 10.1016/s1642-431x(12)60022-9.
In this study, the placental localization of PAG-like transcripts and genomic existence of PAG-like amplicons in new-world (Lp, Lama pacos, alpaca) and old-world camelids (Cb, Camelus bactrianus, bactrian; Cd, Camelus dromedarius; dromedary) are reported for the first time. Sections of Lp (150-347 days post coitum), Cd (43-90 cm crown-rump length) and Cb (term) placentas were used for heterologous (ht; cross-species) autoradiographic in situ hybridization (aISH) with single-stranded diagnostic (antisense) or control (sense) [alpha-(35)S]dATP-labeled 323 nt porcine PAG8 (pPAG8) cDNA probes produced by asymmetric PCRs. The aISH with antisense (35)S-pPAG8 probe identified camelid PAG-like (LpPAG, CbPAG and CdPAG) mRNA expression restricted to chorionic epithelium cells within placentas of camelids. In addition, genomic DNA (gDNA), isolated from placental sections were used as templates for camelid PAG-like gene amplicon production by PCR. Specificity of the obtained multiple camelid gDNA PAG-like amplicons was confirmed by double ht-Southern hybridizations with [alpha-(32)P]dATP-labeled 611 bp pPAG5 and pPAG10 double-stranded cDNA probes. The double ht-Southern hybridizations of camelid gDNA amplicons (with pPAG5 and -10 probes) allowed the identification of length-polymorphism of LpPAG, CbPAG and CdPAG genes, coding catalytically active and potentially inactive forms. Such an application of porcine PAG probes may be advantageous for future identification of still undiscovered PAG-like families in other eutherian species.
在本研究中,首次报道了新世界骆驼科动物(Lp,小羊驼,羊驼)和旧世界骆驼科动物(Cb,双峰驼;Cd,单峰驼)中类PAG转录本的胎盘定位以及类PAG扩增子的基因组存在情况。使用Lp(交配后150 - 347天)、Cd(头臀长43 - 90厘米)和Cb(足月)胎盘的切片,与通过不对称PCR产生的单链诊断(反义)或对照(正义)[α-(35)S]dATP标记的323 nt猪PAG8(pPAG8)cDNA探针进行异源(ht;跨物种)放射自显影原位杂交(aISH)。用反义(35)S - pPAG8探针进行的aISH鉴定出骆驼科动物胎盘绒毛膜上皮细胞中存在类骆驼科动物PAG(LpPAG、CbPAG和CdPAG)mRNA表达。此外,从胎盘切片中分离的基因组DNA(gDNA)被用作通过PCR产生骆驼科动物类PAG基因扩增子的模板。通过与[α-(32)P]dATP标记的611 bp pPAG5和pPAG10双链cDNA探针进行双重ht - Southern杂交,确认了所获得的多个骆驼科动物gDNA类PAG扩增子的特异性。骆驼科动物gDNA扩增子(与pPAG5和 - 10探针)的双重ht - Southern杂交使得能够鉴定LpPAG、CbPAG和CdPAG基因的长度多态性,这些基因编码催化活性和潜在无活性形式。猪PAG探针的这种应用可能有利于未来鉴定其他真兽类物种中尚未发现的类PAG家族。