欢迎访问《茶叶科学》,今天是

大叶龙茶解剖学、肌动蛋白基因及分子标记的研究

  • 徐玲玲 ,
  • 张美云 ,
  • 李同建 ,
  • 秦红霞 ,
  • 赵中伟 ,
  • 樊启水 ,
  • 廖亮 ,
  • 张大明
展开
  • 1. 九江学院生命科学学院,江西 九江 332000;
    2. 江西修水茶叶研究所,江西 修水 332400
徐玲玲(1963— ),女,江西湖口人,教授,主要从事分子生物学研究。

修回日期: 2008-10-23

  录用日期: 2008-12-23

  网络出版日期: 2019-09-09

基金资助

江西省教育厅科技项目,江西省九江市科技项目

Study on Anatomy, Actin Gene and Molecular Marker of Tea Cultivar Dayelong

  • XU Ling-ling ,
  • ZHANG Mei-yun ,
  • LI Tong- jian ,
  • QIN Hong-xia ,
  • ZHAO Zhong-wei ,
  • FAN Qi-shui ,
  • LIAO Liang ,
  • ZHANG Da-ming
Expand
  • 1. College of Life Science, Jiujiang University, Jiujiang 332000, China;
    2. Xiushui tea Research Institute, Xiushui 332400, China

Revised date: 2008-10-23

  Accepted date: 2008-12-23

  Online published: 2019-09-09

摘要

大叶龙茶是来源于江西修水茶科所宁州群体茶园中一株自然突变体形成的大叶并无蕾无性繁殖新品种。对大叶龙茶及其母株的成熟叶片和不同时期的芽进行石蜡切片研究表明,大叶龙茶叶片栅栏组织细胞较长、海绵组织层数增加;大叶龙茶无蕾的原因是由于所有的芽始终保持营养芽的状态所致。首次克隆了茶树3个肌动蛋白基因片段(CS-ACT1,CS-ACT2,CS-ACT3),且都编码225个氨基酸,大叶龙茶与母株及500个BlastX分析获得的肌动蛋白序列在保守结构域F、G、H区有相应的四个氨基酸不同。对大叶龙茶及其母株进行AFLP分析表明,大叶龙茶总带数比母株少,并出现一部分特有带;利用EST-SSR分子标记技术对大叶龙茶及其它常见品种进行研究,表明大叶龙茶等4个修水品种与龙井43有相似的遗传基础。

本文引用格式

徐玲玲 , 张美云 , 李同建 , 秦红霞 , 赵中伟 , 樊启水 , 廖亮 , 张大明 . 大叶龙茶解剖学、肌动蛋白基因及分子标记的研究[J]. 茶叶科学, 2009 , 29(4) : 263 -270 . DOI: 10.13305/j.cnki.jts.2009.4.003

Abstract

Tea Cultivar Dayelong is a vegetative propagation cultivar of large-leaf and budless mutated from a stock plant of Ningzhou population. The paraffin section of mature leaves and buds of different period from Dayelong and its stock plant was investigated. Results showed that the palisade cell was rather long, the layers of spongy cell increased. Dayelong do not have a flower bud is due to all the buds always maintain the situation of vegetative bud. Three actin gene fragments (CS-ACT1, CS-ACT2, CS-ACT3) of tea plant were cloned for the first time. They encoding 225 amino acids. Dayelong, its stock plant and other 500 Actin squences obtained by BlastX analysis showed four amino acids of Dayelong are different from those of corresponding sites on conservative domains F, G and H. The Dayelong and its stock plant for AFLP analysis showed that the band numbers of Dayelong is fewer than the stock plant and has its own specific band. EST-SSR molecular markers technique was used to analyze Dayelong and other cultivars, the results showed that four cultivars of Xiushui including the Dayelong are similar to Longjing 43 in genetic basis.

参考文献

[1] 王柏龄, 张冬燕, 余志成. 自然突变的茶树新株系—大叶龙[J]. 蚕桑茶叶通讯, 1997, (1): 21.
[2] 徐玲玲, 方亮, 廖亮, 等. 自然突变株系——大叶龙茶核型及酯酶同工酶研究[J]. 广西植物, 2003, 23(6): 558~560.
[3] 徐玲玲, 方亮, 廖亮, 等. 自然突变株系—大叶龙茶酯酶同工酶及RAPD分析[J]. 茶叶科学, 2002, 22(1): 87~89.
[4] 刘捷平. 植物形态解剖学[M]. 北京:北京师范学院出版社, 1991, 191~192.
[5] Doyle J J, Doyle J L.A rapid DNA isolation procedure for small quantities of fresh leaf tissue[J]. Phytochemical Bulletin, 1987, 19: 11~15.
[6] 刘雪, 李明顺, 李新海, 等. 利用SSR标记分析玉米群体遗传变异的取样方法[J]. 作物学报, 2005, 31(7): 859~863.
[7] 金冬雁,黎孟枫,等. 分子克隆实验指南(第二版)[M]. 北京: 科学出版社, 1992, 42~60.
[8] Altschul S F, Madden T L, et al. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs[J]. Nucl Acids Res, 1997, 25: 3389~3402.
[9] Vos P, Hogers R, Bleeker M, et al. AFLP: a new technique for DNA fingerprinting[J]. Nucl Acids Res, 1995, 23(21): 4407~4414.
[10] Sun Y, Song W Q, Zhong Y C, ,et al. The use of AFLPs to detect genetic relatedness in Artemia[J]. Electronical Larviculture Newsletter Issue 70. The use of AFLPs to detect genetic relatedness in Artemia[J]. Electronical Larviculture Newsletter Issue 70, 1998, 1 December.
[11] 张峰, 宋文芹, 陈瑞阳. AFLP-银染法检测植物基因组多态性[J]. 细胞生物学杂志, 1999, 21(2): 98~100.
[12] 金基强, 崔海瑞, 龚晓春, 等. 用EST-SSR标记对茶树种质资源的研究[J]. 遗传, 2007, 29(1): 103~108.
[13] 潘根生. 茶树生物学[M]. 北京:中国农业出版社, 2002, 43~49.
[14] Florea C S, Timko M P.Actin genes with unusual organization in the parasitic angiosperm Striga asiatica L. (Kuntze)[J]. Gene, 1997, 186(1): 127~133.
[15] 曹晓风, 王荣臣, 阎隆飞. 豌豆卷须cDNA文库构建及肌动蛋白基因序列分析[J]. 科学通报, 1993, 38: 1804~1808.
[16] Sheterline P, Sharrow J C, Protein Profile: Actin[M]. Academic Press, 1994.
[17] Staiger C J, Schliwa M, Actin localization and function in higher plants[J]. Protoplasma, 1987, 141: 1~12
[18] Rungger D, Rungger-Brandle E, Chaponnier C, et al. Intranuclear injection of anti-actin antibodies into Xenopus oocytes blocks chromosome condensation[J]. Nature, 1979, 282: 320~321.
[19] Scheer U, Hinssen H, Franke W W, et al. Micro-injection of actin-binding proteins and actin antibodies demonstrates involvement of nuclear actin in transcription of lampbrush chromosomes[J]. Cell, 1984, 39: 111~122.
[20] Egly J M, Miyamoto N G, Moncollin V, et al. Is actin a transcription initiation factor for RNA polymerase B[J]. EMBO J, 1984, 3: 2363~2371.
[21] Nakayasu H,Ueda, K.Association of rapidly-labelled RNAs with actin in nuclear matrix from mouse L5178Y cells[J]. Exp Cell Res, 1985, 160: 319~330.
[22] Ueyama H, Nakayasu H, Ueda K.Nuclear actin and transport of RNA[J]. Cell Biol Int Reports, 1987, 11(9): 671~67
文章导航

/