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   <subfield code="a">Structural features of diverse Pin-II proteinase inhibitor genes from Capsicum annuum</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Neha Mahajan, Veena Dewangan, Purushottam Lomate, Rakesh Joshi, Manasi Mishra, Vidya Gupta, Ashok Giri]</subfield>
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   <subfield code="a">Main conclusion : The proteinase inhibitor (PI) genes from Capsicum annuum were characterized with respect to their UTR, introns and promoter elements. The occurrence of PIs with circularly permuted domain organization was evident. Abstract: Several potato inhibitor II (Pin-II) type proteinase inhibitor (PI) genes have been analyzed from Capsicum annuum (L.) with respect to their differential expression during plant defense response. However, complete gene characterization of any of these C. annuum PIs (CanPIs) has not been carried out so far. Complete gene architectures of a previously identified CanPI-7 (Beads-on-string, Type A) and a member of newly isolated Bracelet type B, CanPI-69 are reported in this study. The 5′ UTR (untranslated region), 3′UTR, and intronic sequences of both the CanPI genes were obtained. The genomic sequence of CanPI-7 exhibited, exon 1 (49 base pair, bp) and exon 2 (740bp) interrupted by a 294-bp long type I intron. We noted the occurrence of three multi-domain PIs (CanPI-69, 70, 71) with circularly permuted domain organization. CanPI-69 was found to possess exon 1 (49bp), exon 2 (551bp) and a 584-bp long type I intron. The upstream sequence analysis of CanPI-7 and CanPI-69 predicted various transcription factor-binding sites including TATA and CAAT boxes, hormone-responsive elements (ABRELATERD1, DOFCOREZM, ERELEE4), and a defense-responsive element (WRKY71OS). Binding of transcription factors such as zinc finger motif MADS-box and MYB to the promoter regions was confirmed using electrophoretic mobility shift assay followed by mass spectrometric identification. The 3′ UTR analysis for 25 CanPI genes revealed unique/distinct 3′ UTR sequence for each gene. Structures of three domain CanPIs of type A and B were predicted and further analyzed for their attributes. This investigation of CanPI gene architecture will enable the better understanding of the genetic elements present in CanPIs.</subfield>
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   <subfield code="a">Springer-Verlag Berlin Heidelberg, 2014</subfield>
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   <subfield code="a">Capsicum</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">CanPI</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Gene architecture</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Promoter</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Proteinase inhibitor</subfield>
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   <subfield code="a">CanPI : Capsicum annuum proteinase inhibitor</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">UTR : Untranslated region</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">NPE : Nuclear protein extract</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">EMSA : Electrophoretic mobility shift assay</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">MS : Mass spectrometry</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Mahajan</subfield>
   <subfield code="D">Neha</subfield>
   <subfield code="u">Division of Biochemical Sciences, Plant Molecular Biology Unit, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, 411 008, Pune, Maharashtra, India</subfield>
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   <subfield code="a">Dewangan</subfield>
   <subfield code="D">Veena</subfield>
   <subfield code="u">Division of Biochemical Sciences, Plant Molecular Biology Unit, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, 411 008, Pune, Maharashtra, India</subfield>
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   <subfield code="a">Lomate</subfield>
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   <subfield code="u">Division of Biochemical Sciences, Plant Molecular Biology Unit, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, 411 008, Pune, Maharashtra, India</subfield>
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   <subfield code="a">Gupta</subfield>
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   <subfield code="u">Division of Biochemical Sciences, Plant Molecular Biology Unit, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, 411 008, Pune, Maharashtra, India</subfield>
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   <subfield code="u">Division of Biochemical Sciences, Plant Molecular Biology Unit, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, 411 008, Pune, Maharashtra, India</subfield>
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   <subfield code="t">Planta</subfield>
   <subfield code="d">Springer Berlin Heidelberg</subfield>
   <subfield code="g">241/2(2015-02-01), 319-331</subfield>
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   <subfield code="q">241:2&lt;319</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
   <subfield code="2">nationallicence</subfield>
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