Constructing Cultures Then and Now

Constructing Cultures Then and Now:. Centenary Conference Celebrating Franz Boas and the Jesup North Pacific Expedition 1897-1997. American Museum of Natural History, New York, New York, November 13-17 1997.     

A Novel Tiller Angle Gene,TAC3, together with TAC1 and D2 Largely Determine the Natural Variation of Tiller Angle in Rice Cultivars

Tiller angle is one of the most important components of the ideal plant architecture that can greatly enhance rice grain yield. Understanding the genetic basis of tiller angle and mining favorable alleles will be helpful for breeding new plant-type varieties. Here, we performed genome-wide association studies (GWAS) to identify genes controlling tiller angle using 529 diverse accessions of Oryza sativa including 295 indica and 156 japonica accessions in two environments. We identified 7 common quantitative trait loci (QTLs), including the previously reported major gene Tiller Angle Control 1 (TAC1), in the two environments, 10 and 13 unique QTLs in Hainan and Wuhan, respectively. More QTLs were identified in indica than in japonica, and three major QTLs (qTA3, qTA1b/DWARF2 (D2) and qTA9c/TAC1) were fixed in japonica but segregating in indica, which explained the wider variation observed in indica compared with that in japonica. No common QTLs were identified between the indica and japonica subpopulations. Mutant analysis for the candidate gene of qTA3 on chromosome 3 indicated a novel gene, Tiller Angle Control 3 (TAC3), encoding a conserved hypothetical protein controlling tiller angle. TAC3 is preferentially expressed in the tiller base. The ebisu dwarf (d2) mutant exhibited a decreased tiller angle, in addition to its previously described abnormal phenotype. A nucleotide diversity analysis revealed that TAC3, D2 and TAC1 have been subjected to selection during japonica domestication. A haplotype analysis identified favorable alleles of TAC3, D2 and TAC1, which may be used for breeding plants with an ideal architecture. In conclusion, there is a diverse genetic basis for tiller angle between the two subpopulations, and it is the novel gene TAC3 together with TAC1, D2, and other newly identified genes in this study that controls tiller angle in rice cultivars.     

水稻分蘖角度的QTL定位和主效基因的遗传分析

利用水稻籼粳亚种间组合Asominori×IR24重组自交系(RIL)群体71个株系和相应的全基因组染色体片段置换系(Chromosomesegmentsubstitutionline,CSSL)群体65个株系,在2种环境下对分蘖角度性状进行了数量性状基因座(QTL)定位和上位性效应的遗传分析。在两种群体中都出现了分蘖角度的超亲分离。在RIL群体中发现了5个主效QTLs和3对上位性双位点互作标记基因座,控制水稻分蘖角度。其中在第9染色体上位于XNpb108~C506RFLP分子标记区间的qTA-9基因座在2种环境中同时出现,其贡献率平均为28·6%,增加分蘖角度的等位基因来自籼稻品种IR24。利用CSSL群体图示基因型分析,证实在第9染色体上含有RFLP标记C609和C506约15cM的染色体区段,存在增加分蘖角度的基因,来源于染色体片段供体亲本IR24,在Asominori的遗传背景中能增加分蘖角度约15°,该基因的位置与RIL群体在第9染色体上定位的QTL相同,证实了qTA-9的存在。F1表型测定及F2代遗传分析表明,来自IR24的等位基因是一个不完全显性基因。除一对上位性位点存在显著的环境互作效应外,未发现其他位点存在与环境的互作效应。不同基因的加性效应和双位点的上位性效应的共同作用可能是造成水稻分蘖角度超亲分离的主要原因。     

水稻产量数量性状的遗传调控机制研究进展

粒重、每穗粒数和每株穗数是决定水稻产量的三大要素,也是水稻育种改良的重点．这些性状都是遗传复杂的数量性状．近十年来,水稻数量性状遗传学领域取得了突破性的进展,成功克隆了一批控制水稻产量性状的数量性状位点（QTL）．本文将简要介绍产量性状相关QTL的功能与作用机制．这些研究成果不仅有助于揭示产量性状形成的遗传基础,也将有力推动水稻分子设计育种的进程．     

Then and Now: Reappraising Freedom of the Seas in Modern Law of the Sea

The principle of freedom of the seas remains the governing paradigm of the high seas in modern law of the sea. Although the principle, as embraced by the UN Convention on the Law of the Sea (LOSC), is no longer an absolute norm, it continues to present fundamental challenges for achieving effective conservation on the high seas as it stands in direct contrast to the conservation duty imposed on states by LOSC. The recent UN General Assembly resolution calling for the adoption of a further Implementing Agreement under LOSC to address conservation on the high seas, highlights the need to build a new ethos for management of the high seas, which will require states to loosen their firm grip on the Grotian doctrine. This article seeks to contribute toward shifting attitudes in relation to the principle of freedom through an examination of the nature and scope of the principle in its historic context and in contemporary law of the sea.     

基于CSSL的高密度物理图谱定位水稻分蘖角度QTL

对以籼稻9311为遗传背景携带粳稻日本晴基因组的染色体片段置换系（CSSL）的遗传图谱进行分子标记加密,构建了含250个多态标记的高密度物理图谱。以119个CSSLs为材料,P≤0.001为阈值,筛选到分蘖角度与受体亲本9311差异极显著的10个系。结合物理图谱和代换作图方法,共鉴定出5个分蘖角度QTL,其中qTA11的加性效应表现为增效作用,来源于9311的等位基因;其余4个QTL的加性效应为减效作用,均来源于日本晴的等位基因。qTA6-1和qTA6-2分别被定位于第6染色体RM253–RM527之间的3.55Mb区段和RM3139–RM494的1.65Mb区间;qTA9被定位于第9染色体RM257–RM189之间的3.40Mb区段;qTA10被定位在第10染色体RM222–S10-1之间的2.10Mb区段;qTA11被定位于第11染色体RM1761–RM4504之间的3.30Mb区间。以上研究结果为水稻分蘖角度QTL的精细定位和株型育种提供了依据。     

激素对水稻分蘖芽生长和分蘖相关基因表达的调控效应

以水稻品种‘南粳44＇为材料,研究了植物激素对水稻分蘖芽生长及OsTB1、OsD3、OsD10和OsD27等基因表达的调控。结果表明,水稻分蘖芽生长的调控至少存在两条途径,一条通过调控分蘖芽中CTK含量进而调控OsTB1等基因表达来实现,另一条通过调控OsD3、OsD10和OsD27等系列基因表达来实现。外源IAA和GA_3对水稻分蘖芽生长的调控是通过这两条途径共同实现的。     

稻麦理论分蘖出叶数及其增长公式

稻麦作物分蘖出叶的数值化研究是作物形态发生光合功能等研究的一个重要基础．根据稻麦叶蘖同伸规律,设n为主茎总叶龄,Li为第i次分蘖上的理论出叶数,K为分蘖的最高次数,则Li和K均是n的函数．如果主茎芽鞘节和分蘖的芽鞘节均不发生分蘖,则K=（n-1）/3,L_i=C~i 1_n-2i(i=1,2,…,K）;如果主茎芽鞘节和分蘖鞘节均能发生分蘖,则K'=（n-1）／2,L'_i=C~i 1_n-i,以上K值均只取整数．分蘖与出叶增长的理论公式可用T＝∑sumfromi=0tok()C~i_A-2i（无鞘叶分蘖）或T'=sumfromi=0tok'()C_A-i-1~i,L'=sumfromi=0toK'()C_A-i-1~i,L'=sumfromi=0toK'()C_A-1~i 1（有鞘叶分蘖）来表示．这里T与L（T'与L'）分别为单株总茎蘖数与单株总叶数,A为叶龄．文章还采用数学归纳法对公式进行了数学证明,并展述了可能的应用前景．同样方法可证明莫惠栋等提出的稻麦理论分蘖数计算公式.