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Table 5 Isolated transformants.

From: Reverse genetics in Chlamydomonas: a platform for isolating insertional mutants

Interrupted gene

ID1

Library

Localization and orientation of the insertion2

Deletion size at the genomic region (bp)

Expression of the interrupted gene

Sulfur starvation responsive genes

RDP3

183511

1

5'UTR, +

n.a.

n.a.

AOT4

206110

1

1st exon, +

0

truncated and co-expressed with the marker as a chimeric mRNA

TAUD1

127464

1

2nd intron, +

0

truncated and co-expressed with the marker as a chimeric mRNA. Low expression levels relative to the parental strain

TAUD2

77600

1

3rd exon, -

n.a.

mRNA not detected

HAP3

182794

1

4th exon,+

n.a.

n.a.

PWR1

205514

1

1st exon, +

0

truncated and co-expressed with the marker as a chimeric mRNA.

Sulfate transporter genes

SULTR1 (1)

420357

1

3'UTR, +

8

n.a.

SULTR1 (2)

420357

1

promoter, +

3

n.a.

SULTR1 (3)

420357

1

17th exon, +

0

truncated and co-expressed with the marker as a chimeric mRNA

SULTR2

150514

1

9th exon, -

0

truncated and co-expressed with the marker as chimeric mRNA; transcript has a premature stop codon after splicing

SLT1 (1)

205502

1

8th exon, +

0

truncated and co-expressed with the marker as chimeric mRNA

SLT1 (2)

205502

2

promoter, +

12,000

n.a.

SLT2

205501

1

5'UTR, +

0

low expression levels relative to the parental strain

Hydrogen production and fermentation related genes

PFL1 (1)

206677

1

7th exon, +

0

truncated and co-expressed with the marker as a chimeric mRNA

PFL1 (2)

206677

1

1st intron, -

12

low expression levels relative to the parental strain

PFL1(3)

206677

1

5'UTR, -

0

low expression levels relative to the parental strain

FMR

145357

1

5'UTR, +

n.a.

n.a.

MME4

196831

1

6th exon, +

0

n.a.

HYDA1 (1)

183963

1

5'UTR, +

n.a.

n.a.

HYDA1 (2)

183963

1

3'UTR, -

2

n.a.

HYDA2

24189

1

9th exon, +

0

n.a.

PDC1

193810

1

5th introns, -

n.a

n.a

SEP (1)

147682

1

4th exon, +

0

n.a.

SEP (2)

147682

1

7th exon, +

4

n.a.

NADTH (1)

139758

1

3'UTR, -

0

n.a.

NADTH (2)

139758

1

3'UTR, -

n.a.

n.a.

PDK1

196270

1

3rd intron, +

0

n.a.

H4

163170

1

5'UTR, -

n.a.

n.a.

FDX

188740

1

2nd exon, +

15

n.a.

P4H-2

206683

1

3rd exon, +

0

n.a.

P4H-10

111255

1

7th exon, +

7

n.a.

P4H-10b

182877

1

3'UTR, -

0

n.a.

HCP4

148255

1

3'UTR, -

34

n.a.

ADH1

536345

1

15th exon, -

0

no protein detected

Other processes

RelA/SpoT homolog (1)

419232

1

promoter, +

0

n.a.

RelA/SpoT homolog (2)

419232

1

promoter, +

0

n.a.

AMT1;1

158745

2

3'UTR, -

n.a.

n.a.

CLPD

195417

1

3'UTR, +

n.a.

n.a.

PK2

174928

1

16th exon, +

n.a.

n.a.

WD

524057

1

17th exon, +

0

n.a.

GIP1

34332

1

2nd exon, +

0

n.a.

ABC1

523148

1

3'UTR, +

n.a.

n.a.

ABC2

60710

1

23rd exon, +

n.a.

n.a.

GOX8

196818

1

2nd exon, -

n.a.

n.a.

GOX15

196829

1

16th exon, +

0

n.a.

ATPASE

190023

1

3'UTR, -

1

n.a.

KIN

140337

1

5'UTR, +

n.a.

n.a.

  1. 1Protein IDs from the Joint Genome Institute Chlamydomonas v.4 website. 2Localization and orientation of the inserted marker gene relative to the interrupted target gene: + and - denote the same and opposite orientation, respectively. Independent insertion alleles for the same target gene are indicated by the same gene designation, but with a different number placed in a parenthesis. n.a.: not analyzed.