اگلا جہان
ماپیاں دے گھر سدا نہیں رہنا ہک دن توں ٹر جانا
دم دم رب رب ورد پکا توں ایہہ تیرے کم آنا
ماں تیرا پئی داج بناندی
محنت کر کے پئی پڑھاندی
ہر دم صدقے واری جاندی
اک دن اوسے ماں نے تینوں ڈولی دے وچ پانا
دم دم رب رب ورد پکا توں ایہہ تیرے کم آنا
جوبن وچ مغرور کڑے
کیوں پھرنی ایں لا سندور کڑے
کی کرسیں پیش حضور کڑے
کلم کلیاں اگے جانا اوتھے جا کے توں پچھتانا
دم دم رب رب ورد پکا توں ایہہ تیرے کم آنا
مکھ تیرے تے آئی بہار
جد ویکھن ، رُکدے اسوار
جھلدے نہ اکھیاں دے وار
جوبن ڈھلیا تے تیرے ول کسے نہ مکھ پرتانا
دم دم رب رب ورد پکا توں ایہہ تیرے کم آنا
بلبل کردی موج بہاراں
وچھڑی کونج تے گئیاں ڈاراں
کیہڑا سنگی حشر بزاراں
ویکھ جنازہ ہک دن تیرا بھائیاں چک لے جانا
دم دم رب رب ورد پکا توں ایہہ تیرے کم آنا
ایہہ دنیا بہت سہانی اے
ایتھے چلنی نہیں من مانی اے
دن قادریؔ چار جوانی اے
ہک دن ایسا قادری آسی توں وی صاحب دے ول جانا
دم دم رب رب ورد پکا توں ایہہ تیرے کم آنا
This study focuses on the impact of Religious Education in Pakistan at individual and collective levels. The research discusses the educational basis for the study of religion and analyzes the contribution of religious education towards the intellectual growth of individuals. The study raises few questions regarding religious education in Pakistan such as; why has our education system been divided into religious and secular education system. Whether the existing religious education is able to create a linkage between religion and society or not, if not what are the areas which need to be focused. What are the possibilities of sidelining the religious education and what could be its effects. The research focuses on the aims and objectives or religious education in Pakistan by analyzing the nature of curriculums of religious education at various levels. This study highlights the deficiency of the inclusion of the teachings of other religions in our religious education. The research consists of a current survey of the said topic, some findings and conclusions on the issue and few recommendations as well.
The three dehydrin genes of Eucalyptus species, the dehydrin-1 (EgDHN-1), dehydrin-2 (EgDHN-2) and dehydrin-10 (EgDHN-10) were isolated from local Eucalyptus globulus species for transformation in different varieties of potato for developing abiotic stress tolerance. These three lysine rich dehydrin genes of Eucalyptus have not been reported earlier to be manipulated for genetic engineering or for transformation into a crop plant. The genes were amplified from DNA as well as mRNA (through cDNA). The amplified genes were cloned in TA cloning vector. Cloned dehydrin genes were sequenced and detailed in silico analyses were conducted. Complete sequence of EgDHN-10 gene was obtained from DNA including introns. Coding sequence from its mRNA was also complete and found 92% similar with EgDHN-10 of Eucalyptus globulus after DNA BLAST analyses. The sequencing data of other genes obtained incomplete that showed 99% and 98% homology, after DNA BLAST analyses, with Predicted Eucalyptus grandis Rab18 gene and Eucalyptus globulus EgDHN-1 gene respectively. 297bp long sequence of EgDHN-10 that codes for mature peptide was further sub-cloned in E. coli expression vector pET30a. The sequence was submitted to the NCBI (MG948256.1) and it had extra integration of five electrically charged amino acids (two positively charged Histidine, one negatively charged Glutamate, and two negatively charged Aspartate residues) and one Lysine (K). The presence of one extra K residue is very important for enhanced stress tolerance activity of the transformed dehydrin protein due to its role in functions of K-segments. Presence of more charged amino acids in the binding surface of dehydrin protein enhances its capability to bind with other macromolecules, reactive oxygen species and free metal ions.IPTG induced successful expression of EgDHN-10, cloned in pET30a, was detected in E. coli BL21 ii DE3 strain by protein dot blot analysis. After getting excellent expression of Eucalyptus globulus EgDHN-10 gene outside Eucalyptus cell’s environment, the gene was sub-cloned in pCAMBIA 1301 plant binary vector and transformed into Agrobacterium tumefascience. The nodal regions of three potato cultivars, the Cardinal, Sante and Lady Rosetta, were infected with transformed Agrobacterium (through co-cultivation) carrying EgDHN-10. Putative transgenic plants were first screened by GUS assay and PCR. The successful integration of EgDHN-10 gene in potato genome was confirmed by DNA dot blot analysis. The EgDHN-10 gene’s expression was confirmed from potato mRNA by PCR and real time quantitative PCR. In some plants up to 12 folds DHN 10 expression was observed through qPCR. The acquired abiotic stress tolerance was quantified in stressed transformed potato plants by ion leakage assay (ILA) of cell rupture to select the stable transgenic plants. The stress tolerant transformed plants of Cardinal, Sante and Lady Rosetta were maintained in plant tissue culture setup and pots. The transgenic Sante variety was multiplied and maintained in CAMB trial field in an experiment of growth promoting effect of biofertilizer on trial field plants. The stress tolerant Sante plants showed significant difference over control plants in studied plant growth parameters like plant height, maximum root length, number of roots and number of multiple shoots formation, number and weight of tuber formation.