國產(chǎn)驢蹄草的細胞地理學研究(英文）

王廣艷　周寧　錢敏　張嬋　楊永平

摘 要： ?為探討國產(chǎn)毛茛科（Ranunculaceae）驢蹄草屬（Caltha）兩種植物的演化，該文利用傳統(tǒng)染色體壓片技術和流式細胞術，并結合前人染色體研究結果，對我國驢蹄草23個居群和花葶驢蹄草10個居群進行了細胞學研究。結果表明：驢蹄草是由四倍體（2n=4x=32）、六倍體（2n=6x=48）和八倍體（2n=8x=64）構成的多倍體復合群，花葶驢蹄草具有四倍體（2n=4x=32）和八倍體（2n=8x=64）兩種倍性水平。驢蹄草和花葶驢蹄草均是四倍體較為常見，目前尚未見有二倍體報道。由于驢蹄草和花葶驢蹄草大部分居群采自中國青藏高原地區(qū)，可能在冰期時存在古二倍體，其適應性較弱，逐漸被其他的倍性取代，這是由于不同細胞型對環(huán)境適應性的結果。驢蹄草可能存在兩條進化路線：一條是從甘肅到達云南;另一條是從西藏到達云南。前期分子系統(tǒng)學研究顯示花葶驢蹄草與驢蹄草的親緣關系較近，該研究結果中花葶驢蹄草染色體比驢蹄草要小，花葶驢蹄草可能比驢蹄草相對進化。目前花葶驢蹄草只有10個居群，還需進一步增加居群量來解析其演化路線。

關鍵詞： 細胞地理， 驢蹄草， 花葶驢蹄草， 多倍化

Polyploidy， the duplication of entire sets of chromosomes， is a key process in the evolution and diversification of vascular plants （Hegarty et al.， 2013; Otto & Whitton， 2000）. Previous studies have found that polyploids are better to adapt to stress or novel niches than their diploid progenitors （Ehrendorfer， 1980; Grant， 1981; Levin， 2004; Morton， 1993; Otto & Whitton， 2000; Stebbins， 1985）. Furthermore， intraspecific variation in ploidy level is frequently observed in angiosperms （Kolárˇ et al.， 2015; Wood et al.， 2009）. It is known that polyploidization is one of the few speciation processes that may operate in sympatry， due to the possible immediate emergence of reproductive isolation between individuals with different ploidy levels （Husband & Sabara， 2003）. Therefore， the geographic distribution of cytotypes could provide valuable information about the origin and maintenance of different ploidy levels （Baack， 2004; Kolárˇ et al.， 2009; Rieseberg & Willis， 2007; Segraves et al.， 1999）.

The perennial herb Caltha palustris grows from 600-4 000 m in mountain regions， valleys， marshlands， forests， streams， and on grassy slopes in the north temperate region （Wang et al.， 2001）. After C. palustris was first described by Linnaeus （1753）， great variability of some morphological characters was described in this species， such as plant size， leaf shape and size， leaf margins， flowers， mature follicles， rooting at nodes， tepal number and color， and seed color and symmetry （Smit， 1973; Kumar & Singhal， 2008）. It is previously shown that morphological diversity is a product of environmental conditions （Blagojevic et al.， 2013）. The current study primarily focused on cytotype distribution in the C. palustris complex， which includes tetraploids （Wang et al.， 2013; Yang， 2002; Yuan & Yang， 2006）， hexaploids （Parfenov & Dmitrieva， 1985; Wang et al.， 2013; Yang， 2002; Yuan & Yang， 2006）， and octoploids （Wang et al.， 2013; Yang， 2002; Yuan & Yang， 2006） （x=8， Langlet， 1927）. Furthermore， molecular phylogenetic evidence also shows that C. scaposa is sister to C. palustris （with 100% bootstrap support） （Cheng & Xie， 2014; Schuettpelz & Hoot， 2004）. Caltha scaposa is endemic to SinoHimalaya， and grows from 2 800 to 4 100 m in wet parts of alpine meadows and valleys. Only two cytotypes have been detected： tetraploids （Wang et al.， 2013） and octoploids （Wang et al.， 2013; Yuan & Yang， 2006） （x=8， Langlet， 1927）. The existence of different cytotypes in C. palustris and C. scaposa may indicate strong spatial segregation. As a result of inche differentiation （Ehrendorfer， 1980; Lewis， 1980）， reproductive exclusion （Levin， 1975; VanDijk & BakxSchotman， 1997）， and historical factors （AnCˇev， 2006）， these distinct cytotypes may experience differential reproductive success and occurrence of particular evolutionary constraints or demographic stochasticity （MunozPajares et al.， 2017）.

By conducting a novel analysis of previous cytotype distribution data， we herein present a cytogeographical study of C. palustris and C. scaposa in China. Our aims in this study were as follows： （1） To assess the geographic distribution of different cytotypes in C. palustris and C. scaposa to propose a scenario of dispersal events; （2） To determine the major driving force of speciation in C. palustris and C. scaposa.

1 Materials and Methods

1.1 Taxon sampling

In this study， we sampled six C. palustris accessions and four C. scaposa accessions （Table 1）. In total， 15-20 plants from each population were sampled. Geographical coordinates were recorded in the field using a GPS instrument. Living plants were cultivated in a greenhouse， and voucher specimens were deposited in the herbarium of Kunming Institute of Botany， Chinese Academy of Sciences. We performed cytogeographical analysis using these accessions and previously reported data （Yang， 2002; Yuan & Yang， 2006; Table 2）.

1.2 Chromosome number

Root tips were collected from each individual and pretreated with a solution of 0.002 mol·L1 8hydroxyquinoline at 20-21 ℃ for 4-5 h. After fixation for 50 min in Carnoy’s solution （ethanol∶acetic acid=3∶1） at 4 ℃， the root tips were dissociated in a mixture of 1 N HCl and 45% acetic acid （1∶1） at 60 ℃ for 30 s， stained with 1% acetic orcein for 2-3 h and squashed on a glass slide （Wang et al.， 2013）. Chromosome numbers were determined for each accession from at least 50 cells of at least two seedlings by mitotic observations. Mitotic interphase nuclei and prophase chromosomes preparations followed Tanaka （1971， 1977， 1987）， and the designation of the centromeric position followed Levan et al. （1964）. Karyotype asymmetry was classified according to Stebbins （1971）.

1.3 Flow cytometry and DNA ploidy level determination

Propidium iodide flow cytometry （FCM） analysis was performed using fresh leaf samples from our greenhouse. Approximately 0.5 cm2 of leaf material was finely diced using a new razor blade in a Petri dish that contained 1 500-2 000 μL of WPB nuclear solution buffer （0.2 mol·L1 TrisHCl， 4 mmol·L1 MgCl·6H2O， 2 mmol·L1 EDTA Na2·2H2O， 86 mmol·L1 NaCl， 10 mmol·L1 Na2S2O5， 1% PVP10， 1% [v/v] Triton X100， pH 7.5） （Tian et al.， 2011）. The nuclear suspension was then filtered through disposable filters （30 μm） to remove cell debris， and stained with 150 μL propidium iodide （50 μg·mL1; including RNAse [500 μg·mL1]） for 10 min. Samples were analyzed on a CyFlow Space （Partec， Münster， Germany） flow cytometer equipped with a blue laser operating at 488 nm. At least 5 000 nuclei were measured for each sample. FlowMax ver. 2.82 was used to analyze the resulting histograms. By comparison with a known ploidy level （4x; yyp04）， we estimated the ploidy levels of other samples based on the histograms. The ploidy level of each sample was calculated as described by Tian et al.， 2011：

Ploidy level of sample=（mean of sample peak/mean of standard peak） × ploidy level of the standard species.

2 Results and Analysis

2.1 Chromosome counts and DNA ploidy level determination

In this study， ploidy levels included 13 4x C. palustris， one 6x C. palustris， nine 8x C. palustris， seven 4xC. scaposa， and three 8x C. scaposa accessions （Table 2）; These specimens were collected from Gansu （one accession）， Yunnan （16 accessions）， Sichuan （four accessions）， Tibet （one accession）， Guizhou （one accession）， and Qinghai （one accession）. Metaphase chromosomes of eight accessions are shown in Fig. 1. We successfully estimated the ploidy levels of two C. palustris accessions （yyp09 and yyp10） by FCM at 4x and 8x （Fig. 2）.

2.2 Cytogeography

The ploidy distribution of C. palustris and C. scaposa was revealed based on currently available data. All C. palustris accessions were singleploidy， although our sample was very limited in some accessions; however， secondary constriction chromosomes were observed in three C. palustris accessions （Table 2）. The tetraploid cytotype was more common than the other cytotypes （hexaploids and octoploids）. Moreover， the tetraploid karyotype also exhibited obvious variation among accessions. The samples from Diqing Tibetan Autonomous Prefecture （Yunnan） included tetraploid， hexaploid， and octoploid cytotypes. Two cytotypes （tetraploids and octoploids） were found in Lijiang （Yunnan）. Only one cytotype existed in Tewo （Gansu）， Dali （Yunnan）， Gongshan （Yunnan）， Hongyuan （Sichuan）， Nayong （Guizhou）， and Zuogong （Tibet）. All C. scaposa accessions were singleploidy， and the tetraploid cytotype was also common. Two cytotypes （tetraploids and octoploids） existed in Sichuan， and one cytotype each in Tibet， Qinghai， and Yunnan. In addition， only one contact areas between different cytotypes were detected. In the Xiaozhongdian accession， a region of overlap between the ranges of 4x C. palustris and 8x C. scaposa was observed.

3 Discussion

FCM offers a rapid and precise method for identifying taxa of different ploidy levels， enabling researchers to map the finescale distribution of ploidies within individual populations （Suda et al.， 2004）. FCM has been used in ploidy analysis， e.g.， in Ranunculus （Ranunculaceae） （Cires et al.， 2010） and C. leptosepala s.l. （Wefferling et al.， 2017）. In our study， ploidy levels of two accessions （yyp09 and yyp10） were estimated by FCM. The current study revealed that C. palustris may be viewed as a polyploid complex， which presents clear patterns of cytotype distribution. Polyploidy is a prevalent phenomenon in the chromosomal evolution of extant species and genera （Otto & Whitton， 2000）， and it may have contributed to the origin of flowering plants （De Bodt et al.， 2005）. As a result， plant scientists have recognized that polyploid lineages may have complex relationships with each other and their diploid ancestors， making application of species concepts problematic （Soltis et al.， 2007， 2009）.

C. palustris polyploid complex showed a varied cytotype distribution. No diploids and few hexaploids were found in this study， but tetraploid and octoploid cytotypes were common and widespread. Similarly， in C. scaposa， tetraploids and octoploids were common， whereas diploids and hexaploids were not found. Such distribution patterns are often explained by cytotype adaptive differences to the underlying heterogeneity of environmental factors （Lewis， 1980）. All accessions except for the Guizhou and Gansu accessions were from extreme habitats， like alpine mountains in the QinghaiTibetan Plateau. Polyploidy is common in plants from cold climates with harsh and stressful environments （Grant， 1981; Lve & Lve， 1949， 1967）. Therefore， a relatively high frequency of polyploidy was observed in this species. Ancestral diploids may be present in this region during glacial periods and colonized most regions at the end of the glaciation cycles. However， other ploidy levels could gradually replace diploids， because of their increased fitness in changing environment （Cui et al.， 2008）.

The chromosome counts observed in the C. palustris complex indicate that ploidy changes may be important in its evolution. Chromosome counts often show obvious differences in different accessions within a particular species. Our analysis showed that the Hengduan Mountains could be better viewed as a polyploid complex of diploids， tetraploids， and hexaploids. Symmetrical karyotypes are widely accepted to be more primitive than asymmetrical ones （Stebbins， 1971）. In our combined data （Table 1）， the accessions from Zhongdian （Yunnan） with different types （3B， 3C）， AI （11.39， 7.34， 5.96）， and the secondary constrictions showed the highest asymmetric tendencies. Therefore， we speculate that two possible evolutionary trends may exist： one from Gansu to Yunnan， and the other from Tibet to Yunnan of China.

Molecular phylogeny have shown that C. scaposa is closely related to C. palustris （Cheng & Xie， 2014; Schuettpelz & Hoot， 2004）. C. scaposa cytotype distribution was determined from only ten populations; therefore， C. scaposa cytogeography could not be comprehensively analyzed. Moreover， the chromosome size of this species was smaller than that of C. palustris. The size of the chromosome is also a feature subject to evolutionary change， the direction of chromosome evolution could have a decrease trend in chromosome size （Martel et al.， 2004）. Therefore， smaller chromosomes may be a relatively derived evolutionary character. Consequently， in the future， additional samples need to be analyzed to better elucidate C. scaposa cytogeography.

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