حبیب تنویر کا ڈرامہ " آگرہ بازار"
احمد سہیل
کلیدی لفظیات اوراصطلاحات —: آگرہ بازار،سوانح عمری حبیب تنویر ، نظیر اکبرآبادی، تھیٹر، انڈین تھیٹر، نیا تھیٹر، بشری تہذیب ، تاریخ سازی۔ لسانی تجربات :::
آگرہ میں بازار پر افسردگی کا راج ہے اور کچھ نہیں بکتا۔ ایک کھیرا بیچنے والے کو لگتا ہے کہ اگر اسے اپنی مصنوعات کی خوبیوں کے بارے میں لکھی ہوئی نظم مل جائے تو یہ بہتر فروخت ہوگی۔ وہ کئی شاعروں سے رجوع کرتا ہے لیکن وہ اس کی درخواست کو ٹھکرا دیتے ہیں۔ آخر میں وہ شاعر نظیر کے پاس جاتا ہے جو اسے فوراً پابند کرتا ہے۔ وہ کھیرے کے بارے میں نظیر کا گانا گاتا ہے اور اس کے پروڈکٹ کے لیے گاہک جمع ہوتے ہیں۔ دوسرے دکاندار - لڈو والا، تربوز والا، وغیرہ - اس کی پیروی کرتے ہیں اور جلد ہی پورا بازار نظیر اکبر آبادی کے گانوں سے گونجنے لگتا ہے۔
اس مرکزی پلاٹ کے ارد گرد ایک نوجوان آوارہ کی کہانی بنی ہے جو ایک ویگن کا پیچھا کرتا ہے اور اپنے حریف ایک پولیس انسپکٹر کے ہاتھوں انجام کو پہنچتا ہے، جسے وہ محبت کے اس کھیل میں پہلے شرمندہ کر چکا ہے۔ ٹی اے، ممبئی کے سرگرم رکن ہونے کے علاوہ، وہ ایڈیٹر اور ڈرامہ نقاد بھی رہ چکے ہیں۔ ان کی کچھ اہم پروڈکشن جن میں آگرہ بازار، مٹی کی گاڑی، چرنداس چور، جن لاہور نہیں دیکھا، راجکت اور بہت کچھ شامل ہے۔ حبیب تنویر کو سنگیت ناٹک اکادمی ایوارڈ، ڈرامہ کے لیے شیکھر سمان، ناندیکر ایوارڈ، فرنگ فرسٹ ملا۔
* نیا تھیٹر*
نیا تھیٹرحبیب تنویرنے 1959 میں قائم کیا ۔ ایک پیشہ ور...
Academic-related demands that exceed students’ adaptive capabilities are collectively known as academic stress. High levels of academic stress are associated with an increased likelihood of depression, insomnia, substance addiction, self-harm, suicidal ideation, and subsequently, quitting education. Globally, academic stress is now a common phenomenon due to COVID-19-induced changes in the education system. Knowledge of the magnitude of academic stress and its factors can enable early recognition, intervention, and alleviation of the problem. The objective of this study was to assess the magnitude of perceived academic stress and identify the main stressors through a cross-sectional survey using the Manipal Inventory of Academic Stress scale. The study participants involved 2152 Grade 11 and 12 Commerce students enrolled in 34 pre-university colleges in Poonch AJK. A stratified cluster sampling method was used in the study. Statistical methods, namely descriptive statistics, multiple linear regression analysis, two-sample independent t-test, and one-way ANOVA tests, were used in the study. The study observed that one in every four pre-university students experienced high levels of perceived academic stress.Parent expectations, academic queries from neighbors and relatives, and lack of time for revision were identified as the top three stressors. Gender, grade, and mother’s education were associated with academic stress. Interventions at the individual, family, institutional, and community levels are the need of the hour to safeguard adolescents from negative experiences that might deprive them of wellness in their future.
EXPANSINs are the intrinsic proteins in a plant cell and are involved in disentangling the cellulosic microfibrils of the cell wall. The mechanism of EXPANSIN action is generally concerned with cellular expansion. This family of proteins has also been documented to have tissue specific members. Multiple variants of this protein have been identified in specific tissues, which are temporally regulated and functionally specific. The fiber specific EXPANSINs play a key role in the development of cotton fibers. Various isoforms of EXPANSINs were isolated by screening the cDNA libraries constructed at different developmental stages of cotton (Gossypium hirsutum) and Calotropis procera fibers. Nucleotide sequence analysis of the screened clones helped to identify two major variants in cotton (GhEXPA8 and GhEXPA15) and four EXPANSIN isoforms in fast elongating C. procera fibers. The C. procera CpEXPA3 was selected for further analysis on the basis of its close relatedness with cotton fiber EXPANSINs. The comparative analysis of these EXPANSINs with existing database of the gene family revealed that they belong to the third clade of EXPANSIN A family having two characteristic domains. Eight conserved cysteine residues were found in the N-terminal of the deduced amino acid sequence of GhEXPA8, GhEXPA15 and CpEXPA3, while one was in the signal peptide region. Five tryptophan residues were conserved in C-terminal region of these EXPANSINs. The Amino Acid sequences of GhEXPA8 and GhEXPA15 have 98 % identity, while they have 69.8 % and 69.6 % identity with CpEXPA3 respectively. The presence of the signal anchor sites, the hydrophobic regions and the transmembrane regions at the N-terminus suggested that these proteins are targeted to the cellulosic microfibrils through the secretory pathway. The expression of these variants in different tissues was quantified by real time PCR. The transcripts of GhEXPA8 and GhEXPA15 were observed only in fibers, while CpEXPA3 was found to be transcribed nonspecifically in all tissues of the respective plant. The different transcription patterns of GhEXPA8 and GhEXPA15 at various stages of fiber development indicated that they are functionally different genes. The real time PCR analysis indicated the presence of EXPANSIN variants in developing cotton fibers from 0-15 DPA. The RT-PCR demonstrated that transcripts of LTP3 gene could be detected in developing fibers from 0-20 DPA. A plant expression vector was constructed by fusing LTP3 promoter with a reporter gene (GUS with intron) for in 20Generated by Foxit PDF Creator © Foxit Software http://www.foxitsoftware.com For evaluation only. Masooma Thesis vitro expression assay of the promoter strength and specificity in comparison with 2X35S. Transient expression studies on cultured cotton ovules, sepals, petals and stem revealed that the LTP3 promoter activity was confined only to the trichomes. The GUS gene in the expression cassettes was replaced with GhEXPA8, GhEXPA15 and CpEXPA3 generating six EXPANSIN genes constructs under the two promoters (2X35S and LTP3) with an aim to prolong the EXPANSIN gene expression in developing fibers. The construction of the expression cassettes was verified by DNA sequencing and the constructs were handed over to cotton transformation group at NIBGE for their utilization in fiber modification program.