Nelumbo nucifera

Cloning and characterization of the UBC gene from lotus (Nelumbo nucifera)

Y. Diao, Li, G. L., Yu, A. Q., Zheng, X. W., Xie, K. Q., Wang, Y. W., Zhou, M. Q., Ming, J., Hu, Z. L., Diao, Y., Li, G. L., Yu, A. Q., Zheng, X. W., Xie, K. Q., Wang, Y. W., Zhou, M. Q., Ming, J., and Hu, Z. L., Cloning and characterization of the UBC gene from lotus (Nelumbo nucifera), vol. 15, p. -, 2016.

Protein ubiquitination is extensively involved in the regulation of a considerable number of physiological processes in plant cells. E2 (ubiquitin-conjugating enzyme, UBC), one of the essential enzymes of eukaryotic ubiquitination, catalyzes protein ubiquitination together with E1 and E3. In this study, we cloned four full-length cDNA NnUBCs of Nelumbo nucifera. With the same coding sequence length of 459 bp and coding 153 amino acids, these four genes are highly homologous with the AtUBC1 and AtUBC2 of Arabidopsis thaliana.

Development and characterization of genic-SSR markers from different Asia lotus (Nelumbo nucifera) types by RNA-seq

X. F. Zheng, You, Y. N., Diao, Y., Zheng, X. W., Xie, K. Q., Zhou, M. Q., Hu, Z. L., and Wang, Y. W., Development and characterization of genic-SSR markers from different Asia lotus (Nelumbo nucifera) types by RNA-seq, vol. 14, pp. 11171-11184, 2015.

Nelumbo nucifera is an important economic vegetable and traditional medicine, but available genetic resources remain limited. Next generation sequencing has proven to be a rapid and effective means of identifying genic simple sequence repeat (genic-SSR) markers. This study developed genic-SSRs for N. nucifera using Illumina sequencing technology to assess diversity across cultivated and wild lotus. A total of 105,834 uni-contigs were produced with an average read length of 722 bp. Exactly 11,178 genic-SSR loci were identified in 9523 uni-contigs.

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