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Table 1 Information on the H. perforatum accessions used for flower transcriptome analyses

From: De novo sequencing of the Hypericum perforatum L. flower transcriptome to identify potential genes that are related to plant reproduction sensu lato

Accession

Description

Genealogy

Origin

Ploidy

Apospory

Reproduction

13EU*°

Experimental population

4(F12 X An)1/4

IPK-Gatersleben (D)

2n = 4×

<4%

Sexual

20EU°

Experimental population

4(F12 X An)1/6

IPK-Gatersleben (D)

2n = 4×

<4%

Sexual

36EU*

Experimental population

4(F12 X An)1/9

IPK-Gatersleben (D)

2n = 4×

<4%

Sexual

141EU°

Experimental population

4(F12 X No)1a/39

IPK-Gatersleben (D)

2n = 4×

<4%

Sexual

Hp4/13*

Wild population

n.a.

Feltre (I)

2n = 4×

24%

Facultative apomictic

39EU*

Experimental population

4(F12 X No)1a/1

IPK-Gatersleben (D)

2n = 4×

>96%

Obligate apomictic

222EU°

Experimental population

4(R1C2 X Si)1c/2

IPK-Gatersleben (D)

2n = 4x

>96%

Obligate apomictic

1886US°

Wild population

n.a.

Iron Mountain (USA)

2n = 4x

>96%

Obligate apomictic

1973US*

Wild population

n.a.

Tecumseh (USA)

2n = 4×

>96%

Obligate apomictic

3348EU°

Wild population

n.a.

Hamburg (D)

2n = 4×

>96%

Obligate apomictic

  1. For each plant accession, the origin, ploidy and degree of apomixis are indicated. Accessions marked with *were used for 454 sequencing, while those with °were used for Real-Time RT-qPCR. Apospory expressed as percentage was determined by flow cytometric screening of 48 single seeds. For details on the origin and composition of experimental populations please refer to [18].