[1] 何贵平, 齐明, 程亚平, 等.杉木杂交育种中亲本选配方法的研究[J].江西农业大学学报, 2016, 38(4):646-653.
[2] 何贵平, 齐明.杉木育种策略及应用[M].北京:中国林业出版社, 2017:33-77, 149-174.
[3] 洪舟.杉木杂种优势的分子机理研究[D].南京: 南京林业大学, 2009.
[4] 丁昌俊, 张伟溪, 高暝, 等.不同生长势美洲黑杨转录组差异分析[J].林业科学, 2016, 52(3):47-58.
[5] Birchler J A. In search of molecular basis of heterosis[J]. Plant Cell, 2003, 15(10):2236-2239. doi: 10.1105/tpc.151030
[6] Birchler J A. Reflections on studies of gene expression in aneuploids[J]. Biochemical Journal, 2010, 426 (2) :119-123. doi: 10.1042/BJ20091617
[7] Li Z Y, Zhang T F, Wang S C. Transcriptomic analysis of the highly heterotic maize hybrid Zhengdan 958 and its parents during spikelet and floscule differentiation[J]. Journal of Integrative Agriculture, 2012, 11(11):1783-1793. doi: 10.1016/S2095-3119(12)60183-X
[8] Zhang Y, Han X, Sang J, et al. Transcriptome analysis of immature xylem in the Chinese fir at different developmental phases[J]. Peer J, 2016, 4(17):e2097.doi:10.7717/peerj.2097.
[9] Huang H H, Xu L L, Tong Z K, et al. De novo characterization of the Chinese fir (Cunninghamia lanceolata) transcriptome and analysis of candidate genes involved in cellulose and lignin biosynthesis[J]. BMC Genomics, 2012, 13(1):648-658. doi: 10.1186/1471-2164-13-648
[10] Wang Z J, Chen J H, Liu W D, et al.Transcriptome characteristics and six alternative expressed genes positively correlated with the phase transition of annual cambial activities in Chinese fir (Cunninghamia lanceolata (Lamb.) Hook)[J]. PLOS One, 2013, 8(8):1-14.
[11] Qiu Z, Wan L, Chen T, et al. The regulation of activtity in Chinese fir (Cunninghamia Lanceolata) involves extensive transcriptome remodeling[J]. New Phytologist, 2013, 199(3):708-719. doi: 10.1111/nph.12301
[12] 马智慧.铝胁迫下杉木幼苗的几种生理过程及转录组序列的研究[D].福州: 福建农林大学, 2015.
[13] 李阳.亚硝酸盐对水稻胚性愈伤组织的诱导作用及机制[D].武昌: 武汉大学, 2016.
[14] 丁健.沙棘果肉和种子油脂合成积累及转录表达差异研究[D].哈尔滨: 东北林业大学, 2016.
[15] 冯延芝.杜仲种仁转录组测序及FAD3基因鉴定与功能研究[D].北京: 中国林业科学研究院, 2016.
[16] 翟荣荣.超级稻协优9308根系杂种优势的转录组分析[D].北京: 中国农业科学院, 2013.
[17] 蒋桂雄.油桐种子转录组解析及油脂合成重要基因克隆[D].长沙: 中南林业科技大学, 2014.
[18] 徐进, 李帅, 李火根, 等.鹅掌楸属植物生长旺盛期叶芽基因差异表达与杂种优势关系的分析[J].分子植物育种, 2008, 6(6):1111-1116. doi: 10.3969/j.issn.1672-416X.2008.06.014
[19] 张小蒙, 肖宁, 张洪熙, 等.水稻基因差异表达与杂种优势的关系分析[J].中国农业科学, 2012, 45(7):1235-1245.
[20] 王章奎, 倪中福, 孟凡荣, 等.小麦杂交种及其亲本拔节期根系差基因异表达与杂种优势关系的初步研究[J].中国农业科学, 2003, 36(5):473-479. doi: 10.3321/j.issn:0578-1752.2003.05.002
[21] 张君, 闫冬生, 王丕武, 等.大豆杂交种及其亲本籽粒基因差异表达与杂种优势关系[J].中国油料作物学报, 2010, 32(3):354-361.
[22] Bruce A B. The Mendelian theory of heredity and the augmentation of vigor[J]. Science, 1910, 32(827):627-628.
[23] Shull G H. Duplicate genes for capsule-form in Bursa bursa-pastoris[J]. Molecular and General Genetics, 1914, 12(1):97-149. doi: 10.1007/BF01837282
[24] 叶培忠, 陈岳武, 刘大林, 等.配合力分析在杉木数量遗传学中的应用[J].南京林产工业学院学报, 1981, (3):1-21.
[25] 许晨璐, 孙晓梅, 张守攻.差异基因表达和杂种优势形成机制[J].遗传, 2013, 35(6):714-726.
[26] 邢俊杰, 成志伟, 杨剑, 等.利用基因芯片技术分析水稻杂种优势的分子机理[J].杂交水稻, 2005, 20(4):59-61. doi: 10.3969/j.issn.1005-3956.2005.04.025
[27] Meyer S, Pospisil H, Scholten S. Heterosis associated gene expression in maize embryos 6 days after fertilization exhibits additive, dominant and overdominant pattern[J]. Plant Molecular Biology, 2007, 63(3), 381-391. doi: 10.1007/s11103-006-9095-x
[28] 齐明.杉木育种中GCA与SCA的相对重要性[J].林业科学研究, 1996, 9(5):498-503. doi: 10.3321/j.issn:1001-1498.1996.05.010
[29] Xiao J H, Li J M, Yuan L P, et al.Dominance is the major genetic basis in rice as revealed by QTL analysis using molecular markers[J]. Genetics, 1995, 140(2):745-754.
[30] Yu S B, Li J X, Xu C G, et al. Importance of epistasis as the genetic basis of heterosis in an elite rice hybrid[J]. Proc Natl Acad Sci, USA, 1997, 94(17):9226-9231. doi: 10.1073/pnas.94.17.9226
[31] 庄杰云, 樊叶杨.超显性效应对水稻杂种优势的重要作用[J].中国科学:C辑, 2001, 31(2):106-113.
[32] Meyer S, Pospisil H, Scholten S. Heterosis associated gene expression in maize embryos 6 days after fertilization exhibits additive, dominant and overdominant pattern[J]. Plant Molecular Biology, 2007, 63(3):381-391. doi: 10.1007/s11103-006-9095-x
[33] Hoecker N, Keller B, Muthreich N, et al. Comparison of maize (Zea mays L.) F1-hybrid and parental inbred line primary root transcriptomes suggests organ-specific patterns of non-additive gene expression and conserved expression trends[J]. Genetics, 2008, 179(3):1275-1283. doi: 10.1534/genetics.108.088278