A combined crossbred and purebred selection (CCPS) method, i.e. using crossbred and purebred information, was proposed to achieve genetic response in crossbred animals. Selection index theory was applied to establish a CCPS index. The CCPS was compared with pure-line selection (PLS) and crossbred selection (CS) methods. The genetic correlation between purebred and crossbred performance (r pc ) and crossbred heritability (h£) are crucial factors in the comparison. The CCPS is always better than PLS or CS when a fixed number of purebred progeny is tested. With a fixed total number of purebred and crossbred tested progeny, CCPS is only worse than PLS for very high values of r pc (>0-8). Superiority of CCPS over PLS increases and over CS decreases with decreasing r pc . The larger hj is, relative to purebred heritability (h.p, the more response CS and CCPS will achieve. The robustness of CCPS against inappropriate assumptions on r pc and h,? values was investigated. The expected response is always an overestimate, and the actual response is smaller than the optimal response when r pc is assumed one but the true r pc is smaller. The difference between actual and optimal response increases as r pc decreases but it is small for large r pc values (e.g. <3% for r pc >0-7). The expected response is smaller than the actual response when r pc is large and h^ > h p . Finally, the actual response to CCPS is larger than the optimal response to PLS for positive values for r pc . The main conclusions are: (1) CCPS method is optimal for obtaining genetic response in crossbreds; and (2) CCPS with inappropriate assumptions on r pc and h,? values (e.g. recognizing crossbreds as purebreds) achieves more genetic response than PLS for common values of r pc and crossbred heritability.

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The calmodulin-binding transcription activators (CAMTAs) transcription factor family plays an important role in normal plant growth and development, as well as in biotic and abiotic stress resistance. In this study, we identified seven CAMTA genes across the whole genome of Populus trichocarpa and analyzed the expression patterns of PtCAMTAs in the root and leaf tissues. Promoter cis-element analysis indicated that most CAMTA genes contained stress- or phytohormone-related cis-elements. Quantitative real-time reverse transcription-PCR (qRT-PCR) indicated indicated that PtCAMTAs were induced by mannitol, NaCl, cold stress, pathogenic infection with A. alternata, and phytohormone treatments with abscisic acid, salicylic acid, and methyl jasmonate. We analyzed the expression of homologous genes between P. trichocarpa and P. ussuriensis and alternative splicing forms of PtCAMTA genes under cold stress. We also performed a network interaction analysis for PtCAMTA proteins to predict their interactions and associations. The results of the present study serve as a basis for future functional studies on the Populus CAMTA family.

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Camellia is a well-known ornamental flower native to Southeast of Asia, including regions such as Japan, Korea and South China. However, most species in the genus Camellia are cold sensitive. To elucidate the cold stress responses in camellia plants, we carried out deep transcriptome sequencing of ‘Jiangxue’, a cold-tolerant cultivar of Camellia japonica, and approximately 1,006 million clean reads were generated using Illumina sequencing technology. The assembly of the clean reads produced 367,620 transcripts, including 207,592 unigenes. Overall, 28,038 differentially expressed genes were identified during cold acclimation. Detailed elucidation of responses of transcription factors, protein kinases and plant hormone signalling-related genes described the interplay of signal that allowed the plant to fine-tune cold stress responses. On the basis of global gene regulation of unsaturated fatty acid biosynthesis- and jasmonic acid biosynthesis-related genes, unsaturated fatty acid biosynthesis and jasmonic acid biosynthesis pathways were deduced to be involved in the low temperature responses in C. japonica. These results were supported by the determination of the fatty acid composition and jasmonic acid content. Our results provide insights into the genetic and molecular basis of the responses to cold acclimation in camellia plants.